Canonical Allele Identifier: CA343386286

Gene: ATF6

Linked Data

• MyVariant Identifiers: chr1:g.161761317G>T (hg19) ; chr1:g.161791527G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161791527G>T , CM000663.2:g.161791527G>T	GRCh38
NC_000001.10:g.161761317G>T , CM000663.1:g.161761317G>T	GRCh37
NC_000001.9:g.160027941G>T	NCBI36
NG_029773.1:g.30284G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.474G>T MANE Select	ENSP00000356919.3:p.Arg158Ser
ENST00000679833.1:c.474G>T	ENSP00000505321.1:p.Arg158Ser
ENST00000679853.1:c.474G>T	ENSP00000506149.1:p.Arg158Ser
ENST00000679886.1:c.83-10525G>T	ENSP00000506559.1:n.83-10525G>T
ENST00000680180.1:n.514G>T
ENST00000680462.1:c.474G>T	ENSP00000505583.1:p.Arg158Ser
ENST00000680481.1:c.*97G>T	ENSP00000505919.1:n.*97G>T
ENST00000680633.1:c.276G>T	ENSP00000505371.1:p.Arg92Ser
ENST00000680688.1:c.474G>T	ENSP00000504865.1:p.Arg158Ser
ENST00000681001.1:c.*326G>T	ENSP00000506145.1:n.*326G>T
ENST00000681036.1:c.276G>T	ENSP00000505474.1:p.Arg92Ser
ENST00000681169.1:c.474G>T	ENSP00000505455.1:p.Arg158Ser
ENST00000681187.1:n.514G>T
ENST00000681492.1:c.474G>T	ENSP00000506139.1:p.Arg158Ser
ENST00000681541.1:c.276G>T	ENSP00000506087.1:p.Arg92Ser
ENST00000681557.1:c.*275G>T	ENSP00000506229.1:n.*275G>T
ENST00000681738.1:c.474G>T	ENSP00000505025.1:p.Arg158Ser
ENST00000681779.1:n.524G>T
ENST00000681801.1:c.474G>T	ENSP00000505998.1:p.Arg158Ser
ENST00000681912.1:c.90G>T	ENSP00000505875.1:p.Arg30Ser
ENST00000367942.3:c.474G>T	ENSP00000356919.3:p.Arg158Ser
NM_007348.3:c.474G>T	NP_031374.2:p.Arg158Ser
XM_006711224.1:c.474G>T	XP_006711287.1:p.Arg158Ser
XM_011509308.1:c.474G>T	XP_011507610.1:p.Arg158Ser
XM_011509309.1:c.474G>T	XP_011507611.1:p.Arg158Ser
XM_011509310.1:c.474G>T	XP_011507612.1:p.Arg158Ser
XM_011509310.2:c.474G>T	XP_011507612.1:p.Arg158Ser
NM_007348.4:c.474G>T MANE Select	NP_031374.2:p.Arg158Ser