Canonical Allele Identifier: CA1214065

Gene: ATF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161766387C>T , CM000663.2:g.161766387C>T	GRCh38
NC_000001.10:g.161736177C>T , CM000663.1:g.161736177C>T	GRCh37
NC_000001.9:g.160002801C>T	NCBI36
NG_029773.1:g.5144C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.27C>T MANE Select	ENSP00000356919.3:p.Gly9=
ENST00000679833.1:c.27C>T	ENSP00000505321.1:p.Gly9=
ENST00000679853.1:c.27C>T	ENSP00000506149.1:p.Gly9=
ENST00000679886.1:c.27C>T	ENSP00000506559.1:p.Gly9=
ENST00000680180.1:n.67C>T
ENST00000680462.1:c.27C>T	ENSP00000505583.1:p.Gly9=
ENST00000680481.1:c.27C>T	ENSP00000505919.1:p.Gly9=
ENST00000680633.1:c.-95C>T	ENSP00000505371.1:n.-95C>T
ENST00000680688.1:c.27C>T	ENSP00000504865.1:p.Gly9=
ENST00000681001.1:c.27C>T	ENSP00000506145.1:p.Gly9=
ENST00000681169.1:c.27C>T	ENSP00000505455.1:p.Gly9=
ENST00000681187.1:n.67C>T
ENST00000681492.1:c.27C>T	ENSP00000506139.1:p.Gly9=
ENST00000681557.1:c.27C>T	ENSP00000506229.1:p.Gly9=
ENST00000681738.1:c.27C>T	ENSP00000505025.1:p.Gly9=
ENST00000681779.1:n.77C>T
ENST00000681801.1:c.27C>T	ENSP00000505998.1:p.Gly9=
ENST00000681912.1:c.-86C>T	ENSP00000505875.1:n.-86C>T
ENST00000367942.3:c.27C>T	ENSP00000356919.3:p.Gly9=
NM_007348.3:c.27C>T	NP_031374.2:p.Gly9=
XM_006711224.1:c.27C>T	XP_006711287.1:p.Gly9=
XM_011509308.1:c.27C>T	XP_011507610.1:p.Gly9=
XM_011509309.1:c.27C>T	XP_011507611.1:p.Gly9=
XM_011509310.1:c.27C>T	XP_011507612.1:p.Gly9=
XM_011509310.2:c.27C>T	XP_011507612.1:p.Gly9=
NM_007348.4:c.27C>T MANE Select	NP_031374.2:p.Gly9=