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.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152143635G= , CM000668.2:g.152143635G= | GRCh38 |
| NC_000006.11:g.152464770G= , CM000668.1:g.152464770G= | GRCh37 |
| NC_000006.10:g.152506463G= | NCBI36 |
| NG_012855.1:g.498765C= | |
| NG_012855.2:g.498765C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354674.5:c.1641C= MANE Plus Clinical | ENSP00000346701.4:p.Ser547= | |
| ENST00000367255.10:c.25107C= MANE Select | ENSP00000356224.5:p.Ser8369= | |
| ENST00000423061.6:c.24963C= | ENSP00000396024.1:p.Ser8321= | |
| ENST00000672154.1:c.509C= | ||
| ENST00000672169.1:c.842C= | ||
| ENST00000673173.1:c.891-3474C= | ||
| ENST00000673451.1:c.879C= | ENSP00000500189.1:p.Ser293= | |
| ENST00000341594.9:c.23892C= | ENSP00000341887.6:p.Ser7964= | |
| ENST00000347037.9:n.1855C= | ||
| ENST00000354674.4:c.1641C= | ENSP00000346701.4:p.Ser547= | |
| ENST00000367251.7:c.3942C= | ENSP00000356220.3:p.Ser1314= | |
| ENST00000367255.9:c.25107C= | ENSP00000356224.5:p.Ser8369= | |
| ENST00000367256.9:n.8799C= | ||
| ENST00000367257.8:c.3045C= | ENSP00000356226.4:p.Ser1015= | |
| ENST00000409694.6:n.8691C= | ||
| ENST00000423061.5:c.24963C= | ENSP00000396024.1:p.Ser8321= | |
| ENST00000460912.6:n.1721C= | ||
| ENST00000478916.5:n.4129C= | ||
| ENST00000536990.5:n.1944C= | ||
| ENST00000539504.5:c.1572C= | ENSP00000441052.1:p.Ser524= | |
| NM_033071.3:c.24963C= | NP_149062.1:p.Ser8321= | |
| NM_182961.3:c.25107C= | NP_892006.3:p.Ser8369= | |
| XM_006715407.1:c.25212C= | XP_006715470.1:p.Ser8404= | |
| XM_006715408.1:c.25200C= | XP_006715471.1:p.Ser8400= | |
| XM_006715409.1:c.25191C= | XP_006715472.1:p.Ser8397= | |
| XM_006715410.1:c.25212C= | XP_006715473.1:p.Ser8404= | |
| XM_006715411.1:c.25161C= | XP_006715474.1:p.Ser8387= | |
| XM_006715412.1:c.25197C= | XP_006715475.1:p.Ser8399= | |
| XM_006715413.1:c.25143C= | XP_006715476.1:p.Ser8381= | |
| XM_006715414.1:c.25140C= | XP_006715477.1:p.Ser8380= | |
| XM_006715415.1:c.25143C= | XP_006715478.1:p.Ser8381= | |
| XM_006715416.1:c.25128C= | XP_006715479.1:p.Ser8376= | |
| XM_006715417.1:c.25071C= | XP_006715480.1:p.Ser8357= | |
| XM_006715420.1:c.25059C= | XP_006715483.1:p.Ser8353= | |
| XM_006715421.1:c.25056C= | XP_006715484.1:p.Ser8352= | |
| XM_006715422.1:c.25053C= | XP_006715485.1:p.Ser8351= | |
| XM_006715423.1:c.25212C= | XP_006715486.1:p.Ser8404= | |
| XM_006715424.1:c.25212C= | XP_006715487.1:p.Ser8404= | |
| XM_006715425.1:c.25143C= | XP_006715488.1:p.Ser8381= | |
| XM_011535641.1:c.25209C= | XP_011533943.1:p.Ser8403= | |
| XM_011535642.1:c.25197C= | XP_011533944.1:p.Ser8399= | |
| XM_011535643.1:c.25047C= | XP_011533945.1:p.Ser8349= | |
| XM_011535644.1:c.23487C= | XP_011533946.1:p.Ser7829= | |
| XM_011535645.1:c.22980C= | XP_011533947.1:p.Ser7660= | |
| XM_011535647.1:c.18447C= | XP_011533949.1:p.Ser6149= | |
| NM_001347701.1:c.1713C= | NP_001334630.1:p.Ser571= | |
| NM_001347702.1:c.1641C= | NP_001334631.1:p.Ser547= | |
| XM_006715408.2:c.25200C= | XP_006715471.1:p.Ser8400= | |
| XM_006715410.2:c.25212C= | XP_006715473.1:p.Ser8404= | |
| XM_006715412.2:c.25197C= | XP_006715475.1:p.Ser8399= | |
| XM_006715413.2:c.25143C= | XP_006715476.1:p.Ser8381= | |
| XM_006715415.2:c.25143C= | XP_006715478.1:p.Ser8381= | |
| XM_006715416.2:c.25128C= | XP_006715479.1:p.Ser8376= | |
| XM_006715417.2:c.25071C= | XP_006715480.1:p.Ser8357= | |
| XM_006715420.2:c.25059C= | XP_006715483.1:p.Ser8353= | |
| XM_006715421.2:c.25056C= | XP_006715484.1:p.Ser8352= | |
| XM_006715423.2:c.25212C= | XP_006715486.1:p.Ser8404= | |
| XM_006715424.2:c.25212C= | XP_006715487.1:p.Ser8404= | |
| XM_006715425.2:c.25143C= | XP_006715488.1:p.Ser8381= | |
| XM_011535641.2:c.25209C= | XP_011533943.1:p.Ser8403= | |
| XM_011535642.2:c.25197C= | XP_011533944.1:p.Ser8399= | |
| XM_011535645.2:c.22980C= | XP_011533947.1:p.Ser7660= | |
| XM_017010608.1:c.25212C= | XP_016866097.1:p.Ser8404= | |
| XM_017010609.1:c.25212C= | XP_016866098.1:p.Ser8404= | |
| XM_017010610.1:c.25191C= | XP_016866099.1:p.Ser8397= | |
| XM_017010611.2:c.25185C= | XP_016866100.1:p.Ser8395= | |
| XM_017010612.1:c.25134C= | XP_016866101.1:p.Ser8378= | |
| XM_017010613.1:c.25140C= | XP_016866102.1:p.Ser8380= | |
| XM_017010614.1:c.25056C= | XP_016866103.1:p.Ser8352= | |
| XM_017010615.1:c.24987C= | XP_016866104.1:p.Ser8329= | |
| XM_017010616.1:c.25143C= | XP_016866105.1:p.Ser8381= | |
| XM_017010617.1:c.25140C= | XP_016866106.1:p.Ser8380= | |
| XM_017010618.1:c.25128C= | XP_016866107.1:p.Ser8376= | |
| XM_017010619.1:c.23487C= | XP_016866108.1:p.Ser7829= | |
| NM_182961.4:c.25107C= MANE Select | NP_892006.3:p.Ser8369= | |
| NM_001347701.2:c.1713C= | NP_001334630.1:p.Ser571= | |
| NM_001347702.2:c.1641C= MANE Plus Clinical | NP_001334631.1:p.Ser547= | |
| NM_033071.5:c.24963C= | NP_149062.2:p.Ser8321= |