Canonical Allele Identifier: CA343381179

Gene: ATF6

Linked Data

• dbSNP Id: rs1219177714
• gnomAD v2: 1-161823090-C-G
• gnomAD v3: 1-161853300-C-G
• gnomAD v4: 1-161853300-C-G
• MyVariant Identifiers: chr1:g.161823090C>G (hg19) ; chr1:g.161853300C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853300C>G , CM000663.2:g.161853300C>G	GRCh38
NC_000001.10:g.161823090C>G , CM000663.1:g.161823090C>G	GRCh37
NC_000001.9:g.160089714C>G	NCBI36
NG_029773.1:g.92057C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1510C>G MANE Select	ENSP00000356919.3:p.Gln504Glu
ENST00000679833.1:c.1510C>G	ENSP00000505321.1:p.Gln504Glu
ENST00000679853.1:c.1510C>G	ENSP00000506149.1:p.Gln504Glu
ENST00000679886.1:c.904C>G	ENSP00000506559.1:p.Gln302Glu
ENST00000680180.1:n.1550C>G
ENST00000680462.1:c.1510C>G	ENSP00000505583.1:p.Gln504Glu
ENST00000680481.1:c.*1133C>G	ENSP00000505919.1:n.*1133C>G
ENST00000680688.1:c.1567C>G	ENSP00000504865.1:p.Gln523Glu
ENST00000681001.1:c.*1362C>G	ENSP00000506145.1:n.*1362C>G
ENST00000681036.1:c.1312C>G	ENSP00000505474.1:p.Gln438Glu
ENST00000681169.1:c.*428C>G	ENSP00000505455.1:n.*428C>G
ENST00000681187.1:n.1550C>G
ENST00000681492.1:c.1510C>G	ENSP00000506139.1:p.Gln504Glu
ENST00000681541.1:c.1312C>G	ENSP00000506087.1:p.Gln438Glu
ENST00000681557.1:c.*1311C>G	ENSP00000506229.1:n.*1311C>G
ENST00000681738.1:c.1510C>G	ENSP00000505025.1:p.Gln504Glu
ENST00000681779.1:n.1560C>G
ENST00000681801.1:c.1510C>G	ENSP00000505998.1:p.Gln504Glu
ENST00000681912.1:c.1126C>G	ENSP00000505875.1:p.Gln376Glu
ENST00000367942.3:c.1510C>G	ENSP00000356919.3:p.Gln504Glu
ENST00000476437.1:n.717C>G
NM_007348.3:c.1510C>G	NP_031374.2:p.Gln504Glu
XM_006711224.1:c.1510C>G	XP_006711287.1:p.Gln504Glu
XM_011509308.1:c.1567C>G	XP_011507610.1:p.Gln523Glu
XM_011509309.1:c.1567C>G	XP_011507611.1:p.Gln523Glu
XM_011509310.1:c.1567C>G	XP_011507612.1:p.Gln523Glu
XM_011509310.2:c.1567C>G	XP_011507612.1:p.Gln523Glu
NM_007348.4:c.1510C>G MANE Select	NP_031374.2:p.Gln504Glu