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.152143746C>T , CM000668.2:g.152143746C>T | GRCh38 |
| NC_000006.11:g.152464881C>T , CM000668.1:g.152464881C>T | GRCh37 |
| NC_000006.10:g.152506574C>T | NCBI36 |
| NG_012855.1:g.498654G>A | |
| NG_012855.2:g.498654G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354674.5:c.1530G>A MANE Plus Clinical | ENSP00000346701.4:p.Glu510= | |
| ENST00000367255.10:c.24996G>A MANE Select | ENSP00000356224.5:p.Glu8332= | |
| ENST00000423061.6:c.24852G>A | ENSP00000396024.1:p.Glu8284= | |
| ENST00000672154.1:c.398G>A | ||
| ENST00000672169.1:c.731G>A | ||
| ENST00000673173.1:c.891-3585G>A | ||
| ENST00000673451.1:c.768G>A | ENSP00000500189.1:p.Glu256= | |
| ENST00000341594.9:c.23781G>A | ENSP00000341887.6:p.Glu7927= | |
| ENST00000347037.9:n.1744G>A | ||
| ENST00000354674.4:c.1530G>A | ENSP00000346701.4:p.Glu510= | |
| ENST00000367251.7:c.3831G>A | ENSP00000356220.3:p.Glu1277= | |
| ENST00000367255.9:c.24996G>A | ENSP00000356224.5:p.Glu8332= | |
| ENST00000367256.9:n.8688G>A | ||
| ENST00000367257.8:c.2934G>A | ENSP00000356226.4:p.Glu978= | |
| ENST00000409694.6:n.8580G>A | ||
| ENST00000423061.5:c.24852G>A | ENSP00000396024.1:p.Glu8284= | |
| ENST00000460912.6:n.1610G>A | ||
| ENST00000478916.5:n.4018G>A | ||
| ENST00000536990.5:n.1833G>A | ||
| ENST00000539504.5:c.1461G>A | ENSP00000441052.1:p.Glu487= | |
| NM_033071.3:c.24852G>A | NP_149062.1:p.Glu8284= | |
| NM_182961.3:c.24996G>A | NP_892006.3:p.Glu8332= | |
| XM_006715407.1:c.25101G>A | XP_006715470.1:p.Glu8367= | |
| XM_006715408.1:c.25089G>A | XP_006715471.1:p.Glu8363= | |
| XM_006715409.1:c.25080G>A | XP_006715472.1:p.Glu8360= | |
| XM_006715410.1:c.25101G>A | XP_006715473.1:p.Glu8367= | |
| XM_006715411.1:c.25050G>A | XP_006715474.1:p.Glu8350= | |
| XM_006715412.1:c.25086G>A | XP_006715475.1:p.Glu8362= | |
| XM_006715413.1:c.25032G>A | XP_006715476.1:p.Glu8344= | |
| XM_006715414.1:c.25029G>A | XP_006715477.1:p.Glu8343= | |
| XM_006715415.1:c.25032G>A | XP_006715478.1:p.Glu8344= | |
| XM_006715416.1:c.25017G>A | XP_006715479.1:p.Glu8339= | |
| XM_006715417.1:c.24960G>A | XP_006715480.1:p.Glu8320= | |
| XM_006715420.1:c.24948G>A | XP_006715483.1:p.Glu8316= | |
| XM_006715421.1:c.24945G>A | XP_006715484.1:p.Glu8315= | |
| XM_006715422.1:c.24942G>A | XP_006715485.1:p.Glu8314= | |
| XM_006715423.1:c.25101G>A | XP_006715486.1:p.Glu8367= | |
| XM_006715424.1:c.25101G>A | XP_006715487.1:p.Glu8367= | |
| XM_006715425.1:c.25032G>A | XP_006715488.1:p.Glu8344= | |
| XM_011535641.1:c.25098G>A | XP_011533943.1:p.Glu8366= | |
| XM_011535642.1:c.25086G>A | XP_011533944.1:p.Glu8362= | |
| XM_011535643.1:c.24936G>A | XP_011533945.1:p.Glu8312= | |
| XM_011535644.1:c.23376G>A | XP_011533946.1:p.Glu7792= | |
| XM_011535645.1:c.22869G>A | XP_011533947.1:p.Glu7623= | |
| XM_011535647.1:c.18336G>A | XP_011533949.1:p.Glu6112= | |
| NM_001347701.1:c.1602G>A | NP_001334630.1:p.Glu534= | |
| NM_001347702.1:c.1530G>A | NP_001334631.1:p.Glu510= | |
| XM_006715408.2:c.25089G>A | XP_006715471.1:p.Glu8363= | |
| XM_006715410.2:c.25101G>A | XP_006715473.1:p.Glu8367= | |
| XM_006715412.2:c.25086G>A | XP_006715475.1:p.Glu8362= | |
| XM_006715413.2:c.25032G>A | XP_006715476.1:p.Glu8344= | |
| XM_006715415.2:c.25032G>A | XP_006715478.1:p.Glu8344= | |
| XM_006715416.2:c.25017G>A | XP_006715479.1:p.Glu8339= | |
| XM_006715417.2:c.24960G>A | XP_006715480.1:p.Glu8320= | |
| XM_006715420.2:c.24948G>A | XP_006715483.1:p.Glu8316= | |
| XM_006715421.2:c.24945G>A | XP_006715484.1:p.Glu8315= | |
| XM_006715423.2:c.25101G>A | XP_006715486.1:p.Glu8367= | |
| XM_006715424.2:c.25101G>A | XP_006715487.1:p.Glu8367= | |
| XM_006715425.2:c.25032G>A | XP_006715488.1:p.Glu8344= | |
| XM_011535641.2:c.25098G>A | XP_011533943.1:p.Glu8366= | |
| XM_011535642.2:c.25086G>A | XP_011533944.1:p.Glu8362= | |
| XM_011535645.2:c.22869G>A | XP_011533947.1:p.Glu7623= | |
| XM_017010608.1:c.25101G>A | XP_016866097.1:p.Glu8367= | |
| XM_017010609.1:c.25101G>A | XP_016866098.1:p.Glu8367= | |
| XM_017010610.1:c.25080G>A | XP_016866099.1:p.Glu8360= | |
| XM_017010611.2:c.25074G>A | XP_016866100.1:p.Glu8358= | |
| XM_017010612.1:c.25023G>A | XP_016866101.1:p.Glu8341= | |
| XM_017010613.1:c.25029G>A | XP_016866102.1:p.Glu8343= | |
| XM_017010614.1:c.24945G>A | XP_016866103.1:p.Glu8315= | |
| XM_017010615.1:c.24876G>A | XP_016866104.1:p.Glu8292= | |
| XM_017010616.1:c.25032G>A | XP_016866105.1:p.Glu8344= | |
| XM_017010617.1:c.25029G>A | XP_016866106.1:p.Glu8343= | |
| XM_017010618.1:c.25017G>A | XP_016866107.1:p.Glu8339= | |
| XM_017010619.1:c.23376G>A | XP_016866108.1:p.Glu7792= | |
| NM_182961.4:c.24996G>A MANE Select | NP_892006.3:p.Glu8332= | |
| NM_001347701.2:c.1602G>A | NP_001334630.1:p.Glu534= | |
| NM_001347702.2:c.1530G>A MANE Plus Clinical | NP_001334631.1:p.Glu510= | |
| NM_033071.5:c.24852G>A | NP_149062.2:p.Glu8284= |