Canonical Allele Identifier: CA2746386508

Gene: ATF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161791614_161791615insAGA , CM000663.2:g.161791614_161791615insAGA	GRCh38
NC_000001.10:g.161761404_161761405insAGA , CM000663.1:g.161761404_161761405insAGA	GRCh37
NC_000001.9:g.160028028_160028029insAGA	NCBI36
NG_029773.1:g.30371_30372insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.484+77_484+78insAGA MANE Select	ENSP00000356919.3:n.484+77_484+78insAGA
ENST00000679833.1:c.484+77_484+78insAGA	ENSP00000505321.1:n.484+77_484+78insAGA
ENST00000679853.1:c.484+77_484+78insAGA	ENSP00000506149.1:n.484+77_484+78insAGA
ENST00000679886.1:c.83-10438_83-10437insAGA	ENSP00000506559.1:n.83-10438_83-10437insAGA
ENST00000680180.1:n.524+77_524+78insAGA
ENST00000680462.1:c.484+77_484+78insAGA	ENSP00000505583.1:n.484+77_484+78insAGA
ENST00000680481.1:c.*107+77_*107+78insAGA	ENSP00000505919.1:n.*107+77_*107+78insAGA
ENST00000680633.1:c.286+77_286+78insAGA	ENSP00000505371.1:n.286+77_286+78insAGA
ENST00000680688.1:c.484+77_484+78insAGA	ENSP00000504865.1:n.484+77_484+78insAGA
ENST00000681001.1:c.*336+77_*336+78insAGA	ENSP00000506145.1:n.*336+77_*336+78insAGA
ENST00000681036.1:c.286+77_286+78insAGA	ENSP00000505474.1:n.286+77_286+78insAGA
ENST00000681169.1:c.484+77_484+78insAGA	ENSP00000505455.1:n.484+77_484+78insAGA
ENST00000681187.1:n.524+77_524+78insAGA
ENST00000681492.1:c.484+77_484+78insAGA	ENSP00000506139.1:n.484+77_484+78insAGA
ENST00000681541.1:c.286+77_286+78insAGA	ENSP00000506087.1:n.286+77_286+78insAGA
ENST00000681557.1:c.*285+77_*285+78insAGA	ENSP00000506229.1:n.*285+77_*285+78insAGA
ENST00000681738.1:c.484+77_484+78insAGA	ENSP00000505025.1:n.484+77_484+78insAGA
ENST00000681779.1:n.534+77_534+78insAGA
ENST00000681801.1:c.484+77_484+78insAGA	ENSP00000505998.1:n.484+77_484+78insAGA
ENST00000681912.1:c.100+77_100+78insAGA	ENSP00000505875.1:n.100+77_100+78insAGA
ENST00000367942.3:c.484+77_484+78insAGA	ENSP00000356919.3:n.484+77_484+78insAGA
NM_007348.3:c.484+77_484+78insAGA	NP_031374.2:n.484+77_484+78insAGA
XM_006711224.1:c.484+77_484+78insAGA	XP_006711287.1:n.484+77_484+78insAGA
XM_011509308.1:c.484+77_484+78insAGA	XP_011507610.1:n.484+77_484+78insAGA
XM_011509309.1:c.484+77_484+78insAGA	XP_011507611.1:n.484+77_484+78insAGA
XM_011509310.1:c.484+77_484+78insAGA	XP_011507612.1:n.484+77_484+78insAGA
XM_011509310.2:c.484+77_484+78insAGA	XP_011507612.1:n.484+77_484+78insAGA
NM_007348.4:c.484+77_484+78insAGA MANE Select	NP_031374.2:n.484+77_484+78insAGA