Canonical Allele Identifier: CA343384548
Gene: ATF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161781999G>C , CM000663.2:g.161781999G>C GRCh38
NC_000001.10:g.161751789G>C , CM000663.1:g.161751789G>C GRCh37
NC_000001.9:g.160018413G>C NCBI36
NG_029773.1:g.20756G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367942.4:c.247G>C MANE Select ENSP00000356919.3:p.Val83Leu
ENST00000679833.1:c.247G>C ENSP00000505321.1:p.Val83Leu
ENST00000679853.1:c.247G>C ENSP00000506149.1:p.Val83Leu
ENST00000679886.1:c.82+15557G>C ENSP00000506559.1:n.82+15557G>C
ENST00000680180.1:n.287G>C
ENST00000680462.1:c.247G>C ENSP00000505583.1:p.Val83Leu
ENST00000680481.1:c.247G>C ENSP00000505919.1:p.Gly83Arg
ENST00000680633.1:c.49G>C ENSP00000505371.1:p.Val17Leu
ENST00000680688.1:c.247G>C ENSP00000504865.1:p.Val83Leu
ENST00000681001.1:c.*99G>C ENSP00000506145.1:n.*99G>C
ENST00000681036.1:c.49G>C ENSP00000505474.1:p.Val17Leu
ENST00000681169.1:c.247G>C ENSP00000505455.1:p.Val83Leu
ENST00000681187.1:n.287G>C
ENST00000681492.1:c.247G>C ENSP00000506139.1:p.Val83Leu
ENST00000681541.1:c.49G>C ENSP00000506087.1:p.Val17Leu
ENST00000681557.1:c.*48G>C ENSP00000506229.1:n.*48G>C
ENST00000681738.1:c.247G>C ENSP00000505025.1:p.Val83Leu
ENST00000681779.1:n.297G>C
ENST00000681801.1:c.247G>C ENSP00000505998.1:p.Val83Leu
ENST00000681912.1:c.-30-9409G>C ENSP00000505875.1:n.-30-9409G>C
ENST00000367942.3:c.247G>C ENSP00000356919.3:p.Val83Leu
NM_007348.3:c.247G>C NP_031374.2:p.Val83Leu
XM_006711224.1:c.247G>C XP_006711287.1:p.Val83Leu
XM_011509308.1:c.247G>C XP_011507610.1:p.Val83Leu
XM_011509309.1:c.247G>C XP_011507611.1:p.Val83Leu
XM_011509310.1:c.247G>C XP_011507612.1:p.Val83Leu
XM_011509310.2:c.247G>C XP_011507612.1:p.Val83Leu
NM_007348.4:c.247G>C MANE Select NP_031374.2:p.Val83Leu