UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152141208G>C , CM000668.2:g.152141208G>C | GRCh38 |
| NC_000006.11:g.152462343G>C , CM000668.1:g.152462343G>C | GRCh37 |
| NC_000006.10:g.152504036G>C | NCBI36 |
| NG_012855.1:g.501192C>G | |
| NG_012855.2:g.501192C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354674.5:c.1775C>G MANE Plus Clinical | ENSP00000346701.4:p.Thr592Arg | |
| ENST00000367255.10:c.25241C>G MANE Select | ENSP00000356224.5:p.Thr8414Arg | |
| ENST00000423061.6:c.25097C>G | ENSP00000396024.1:p.Thr8366Arg | |
| ENST00000672154.1:c.643C>G | ||
| ENST00000672169.1:c.976C>G | ||
| ENST00000673173.1:c.891-1047C>G | ||
| ENST00000673451.1:c.1013C>G | ENSP00000500189.1:p.Thr338Arg | |
| ENST00000341594.9:c.24026C>G | ENSP00000341887.6:p.Thr8009Arg | |
| ENST00000347037.9:n.1989C>G | ||
| ENST00000354674.4:c.1775C>G | ENSP00000346701.4:p.Thr592Arg | |
| ENST00000367251.7:c.4076C>G | ENSP00000356220.3:p.Thr1359Arg | |
| ENST00000367255.9:c.25241C>G | ENSP00000356224.5:p.Thr8414Arg | |
| ENST00000367256.9:n.8933C>G | ||
| ENST00000367257.8:c.3179C>G | ENSP00000356226.4:p.Thr1060Arg | |
| ENST00000409694.6:n.8825C>G | ||
| ENST00000423061.5:c.25097C>G | ENSP00000396024.1:p.Thr8366Arg | |
| ENST00000460912.6:n.1855C>G | ||
| ENST00000478916.5:n.4263C>G | ||
| ENST00000536990.5:n.2078C>G | ||
| ENST00000539504.5:c.1706C>G | ENSP00000441052.1:p.Thr569Arg | |
| NM_033071.3:c.25097C>G | NP_149062.1:p.Thr8366Arg | |
| NM_182961.3:c.25241C>G | NP_892006.3:p.Thr8414Arg | |
| XM_006715407.1:c.25346C>G | XP_006715470.1:p.Thr8449Arg | |
| XM_006715408.1:c.25334C>G | XP_006715471.1:p.Thr8445Arg | |
| XM_006715409.1:c.25325C>G | XP_006715472.1:p.Thr8442Arg | |
| XM_006715410.1:c.25346C>G | XP_006715473.1:p.Thr8449Arg | |
| XM_006715411.1:c.25295C>G | XP_006715474.1:p.Thr8432Arg | |
| XM_006715412.1:c.25331C>G | XP_006715475.1:p.Thr8444Arg | |
| XM_006715413.1:c.25277C>G | XP_006715476.1:p.Thr8426Arg | |
| XM_006715414.1:c.25274C>G | XP_006715477.1:p.Thr8425Arg | |
| XM_006715415.1:c.25277C>G | XP_006715478.1:p.Thr8426Arg | |
| XM_006715416.1:c.25262C>G | XP_006715479.1:p.Thr8421Arg | |
| XM_006715417.1:c.25205C>G | XP_006715480.1:p.Thr8402Arg | |
| XM_006715420.1:c.25193C>G | XP_006715483.1:p.Thr8398Arg | |
| XM_006715421.1:c.25190C>G | XP_006715484.1:p.Thr8397Arg | |
| XM_006715422.1:c.25187C>G | XP_006715485.1:p.Thr8396Arg | |
| XM_006715423.1:c.25346C>G | XP_006715486.1:p.Thr8449Arg | |
| XM_006715424.1:c.25346C>G | XP_006715487.1:p.Thr8449Arg | |
| XM_006715425.1:c.25277C>G | XP_006715488.1:p.Thr8426Arg | |
| XM_011535641.1:c.25343C>G | XP_011533943.1:p.Thr8448Arg | |
| XM_011535642.1:c.25331C>G | XP_011533944.1:p.Thr8444Arg | |
| XM_011535643.1:c.25181C>G | XP_011533945.1:p.Thr8394Arg | |
| XM_011535644.1:c.23621C>G | XP_011533946.1:p.Thr7874Arg | |
| XM_011535645.1:c.23114C>G | XP_011533947.1:p.Thr7705Arg | |
| XM_011535647.1:c.18581C>G | XP_011533949.1:p.Thr6194Arg | |
| NM_001347701.1:c.1847C>G | NP_001334630.1:p.Thr616Arg | |
| NM_001347702.1:c.1775C>G | NP_001334631.1:p.Thr592Arg | |
| XM_006715408.2:c.25334C>G | XP_006715471.1:p.Thr8445Arg | |
| XM_006715410.2:c.25346C>G | XP_006715473.1:p.Thr8449Arg | |
| XM_006715412.2:c.25331C>G | XP_006715475.1:p.Thr8444Arg | |
| XM_006715413.2:c.25277C>G | XP_006715476.1:p.Thr8426Arg | |
| XM_006715415.2:c.25277C>G | XP_006715478.1:p.Thr8426Arg | |
| XM_006715416.2:c.25262C>G | XP_006715479.1:p.Thr8421Arg | |
| XM_006715417.2:c.25205C>G | XP_006715480.1:p.Thr8402Arg | |
| XM_006715420.2:c.25193C>G | XP_006715483.1:p.Thr8398Arg | |
| XM_006715421.2:c.25190C>G | XP_006715484.1:p.Thr8397Arg | |
| XM_006715423.2:c.25346C>G | XP_006715486.1:p.Thr8449Arg | |
| XM_006715424.2:c.25346C>G | XP_006715487.1:p.Thr8449Arg | |
| XM_006715425.2:c.25277C>G | XP_006715488.1:p.Thr8426Arg | |
| XM_011535641.2:c.25343C>G | XP_011533943.1:p.Thr8448Arg | |
| XM_011535642.2:c.25331C>G | XP_011533944.1:p.Thr8444Arg | |
| XM_011535645.2:c.23114C>G | XP_011533947.1:p.Thr7705Arg | |
| XM_017010608.1:c.25346C>G | XP_016866097.1:p.Thr8449Arg | |
| XM_017010609.1:c.25346C>G | XP_016866098.1:p.Thr8449Arg | |
| XM_017010610.1:c.25325C>G | XP_016866099.1:p.Thr8442Arg | |
| XM_017010611.2:c.25319C>G | XP_016866100.1:p.Thr8440Arg | |
| XM_017010612.1:c.25268C>G | XP_016866101.1:p.Thr8423Arg | |
| XM_017010613.1:c.25274C>G | XP_016866102.1:p.Thr8425Arg | |
| XM_017010614.1:c.25190C>G | XP_016866103.1:p.Thr8397Arg | |
| XM_017010615.1:c.25121C>G | XP_016866104.1:p.Thr8374Arg | |
| XM_017010616.1:c.25277C>G | XP_016866105.1:p.Thr8426Arg | |
| XM_017010617.1:c.25274C>G | XP_016866106.1:p.Thr8425Arg | |
| XM_017010618.1:c.25262C>G | XP_016866107.1:p.Thr8421Arg | |
| XM_017010619.1:c.23621C>G | XP_016866108.1:p.Thr7874Arg | |
| NM_182961.4:c.25241C>G MANE Select | NP_892006.3:p.Thr8414Arg | |
| NM_001347701.2:c.1847C>G | NP_001334630.1:p.Thr616Arg | |
| NM_001347702.2:c.1775C>G MANE Plus Clinical | NP_001334631.1:p.Thr592Arg | |
| NM_033071.5:c.25097C>G | NP_149062.2:p.Thr8366Arg |