Canonical Allele Identifier: CA1202884014

Gene: ATF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161781984A= , CM000663.2:g.161781984A=	GRCh38
NC_000001.10:g.161751774A= , CM000663.1:g.161751774A=	GRCh37
NC_000001.9:g.160018398A=	NCBI36
NG_029773.1:g.20741A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.232A= MANE Select	ENSP00000356919.3:p.Asn78=
ENST00000679833.1:c.232A=	ENSP00000505321.1:p.Asn78=
ENST00000679853.1:c.232A=	ENSP00000506149.1:p.Asn78=
ENST00000679886.1:c.82+15542A=	ENSP00000506559.1:n.82+15542A=
ENST00000680180.1:n.272A=
ENST00000680462.1:c.232A=	ENSP00000505583.1:p.Asn78=
ENST00000680481.1:c.232A=	ENSP00000505919.1:p.Asn78=
ENST00000680633.1:c.34A=	ENSP00000505371.1:p.Asn12=
ENST00000680688.1:c.232A=	ENSP00000504865.1:p.Asn78=
ENST00000681001.1:c.*84A=	ENSP00000506145.1:n.*84A=
ENST00000681036.1:c.34A=	ENSP00000505474.1:p.Asn12=
ENST00000681169.1:c.232A=	ENSP00000505455.1:p.Asn78=
ENST00000681187.1:n.272A=
ENST00000681492.1:c.232A=	ENSP00000506139.1:p.Asn78=
ENST00000681541.1:c.34A=	ENSP00000506087.1:p.Asn12=
ENST00000681557.1:c.*33A=	ENSP00000506229.1:n.*33A=
ENST00000681738.1:c.232A=	ENSP00000505025.1:p.Asn78=
ENST00000681779.1:n.282A=
ENST00000681801.1:c.232A=	ENSP00000505998.1:p.Asn78=
ENST00000681912.1:c.-30-9424A=	ENSP00000505875.1:n.-30-9424A=
ENST00000367942.3:c.232A=	ENSP00000356919.3:p.Asn78=
NM_007348.3:c.232A=	NP_031374.2:p.Asn78=
XM_006711224.1:c.232A=	XP_006711287.1:p.Asn78=
XM_011509308.1:c.232A=	XP_011507610.1:p.Asn78=
XM_011509309.1:c.232A=	XP_011507611.1:p.Asn78=
XM_011509310.1:c.232A=	XP_011507612.1:p.Asn78=
XM_011509310.2:c.232A=	XP_011507612.1:p.Asn78=
NM_007348.4:c.232A= MANE Select	NP_031374.2:p.Asn78=