Canonical Allele Identifier: CA1202913039

Gene: ATF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853241G= , CM000663.2:g.161853241G=	GRCh38
NC_000001.10:g.161823031G= , CM000663.1:g.161823031G=	GRCh37
NC_000001.9:g.160089655G=	NCBI36
NG_029773.1:g.91998G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1451G= MANE Select	ENSP00000356919.3:p.Arg484=
ENST00000679833.1:c.1451G=	ENSP00000505321.1:p.Arg484=
ENST00000679853.1:c.1451G=	ENSP00000506149.1:p.Arg484=
ENST00000679886.1:c.845G=	ENSP00000506559.1:p.Arg282=
ENST00000680180.1:n.1491G=
ENST00000680462.1:c.1451G=	ENSP00000505583.1:p.Arg484=
ENST00000680481.1:c.*1074G=	ENSP00000505919.1:n.*1074G=
ENST00000680688.1:c.1508G=	ENSP00000504865.1:p.Arg503=
ENST00000681001.1:c.*1303G=	ENSP00000506145.1:n.*1303G=
ENST00000681036.1:c.1253G=	ENSP00000505474.1:p.Arg418=
ENST00000681169.1:c.*369G=	ENSP00000505455.1:n.*369G=
ENST00000681187.1:n.1491G=
ENST00000681492.1:c.1451G=	ENSP00000506139.1:p.Arg484=
ENST00000681541.1:c.1253G=	ENSP00000506087.1:p.Arg418=
ENST00000681557.1:c.*1252G=	ENSP00000506229.1:n.*1252G=
ENST00000681738.1:c.1451G=	ENSP00000505025.1:p.Arg484=
ENST00000681779.1:n.1501G=
ENST00000681801.1:c.1451G=	ENSP00000505998.1:p.Arg484=
ENST00000681912.1:c.1067G=	ENSP00000505875.1:p.Arg356=
ENST00000367942.3:c.1451G=	ENSP00000356919.3:p.Arg484=
ENST00000476437.1:n.658G=
NM_007348.3:c.1451G=	NP_031374.2:p.Arg484=
XM_006711224.1:c.1451G=	XP_006711287.1:p.Arg484=
XM_011509308.1:c.1508G=	XP_011507610.1:p.Arg503=
XM_011509309.1:c.1508G=	XP_011507611.1:p.Arg503=
XM_011509310.1:c.1508G=	XP_011507612.1:p.Arg503=
XM_011509310.2:c.1508G=	XP_011507612.1:p.Arg503=
NM_007348.4:c.1451G= MANE Select	NP_031374.2:p.Arg484=