Canonical Allele Identifier: CA2746386562

Gene: ATF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161791706_161791707insACT , CM000663.2:g.161791706_161791707insACT	GRCh38
NC_000001.10:g.161761496_161761497insACT , CM000663.1:g.161761496_161761497insACT	GRCh37
NC_000001.9:g.160028120_160028121insACT	NCBI36
NG_029773.1:g.30463_30464insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.484+169_484+170insACT MANE Select	ENSP00000356919.3:n.484+169_484+170insACT
ENST00000679833.1:c.484+169_484+170insACT	ENSP00000505321.1:n.484+169_484+170insACT
ENST00000679853.1:c.484+169_484+170insACT	ENSP00000506149.1:n.484+169_484+170insACT
ENST00000679886.1:c.83-10346_83-10345insACT	ENSP00000506559.1:n.83-10346_83-10345insACT
ENST00000680180.1:n.524+169_524+170insACT
ENST00000680462.1:c.484+169_484+170insACT	ENSP00000505583.1:n.484+169_484+170insACT
ENST00000680481.1:c.*107+169_*107+170insACT	ENSP00000505919.1:n.*107+169_*107+170insACT
ENST00000680633.1:c.286+169_286+170insACT	ENSP00000505371.1:n.286+169_286+170insACT
ENST00000680688.1:c.484+169_484+170insACT	ENSP00000504865.1:n.484+169_484+170insACT
ENST00000681001.1:c.*336+169_*336+170insACT	ENSP00000506145.1:n.*336+169_*336+170insACT
ENST00000681036.1:c.286+169_286+170insACT	ENSP00000505474.1:n.286+169_286+170insACT
ENST00000681169.1:c.484+169_484+170insACT	ENSP00000505455.1:n.484+169_484+170insACT
ENST00000681187.1:n.524+169_524+170insACT
ENST00000681492.1:c.484+169_484+170insACT	ENSP00000506139.1:n.484+169_484+170insACT
ENST00000681541.1:c.286+169_286+170insACT	ENSP00000506087.1:n.286+169_286+170insACT
ENST00000681557.1:c.*285+169_*285+170insACT	ENSP00000506229.1:n.*285+169_*285+170insACT
ENST00000681738.1:c.484+169_484+170insACT	ENSP00000505025.1:n.484+169_484+170insACT
ENST00000681779.1:n.534+169_534+170insACT
ENST00000681801.1:c.484+169_484+170insACT	ENSP00000505998.1:n.484+169_484+170insACT
ENST00000681912.1:c.100+169_100+170insACT	ENSP00000505875.1:n.100+169_100+170insACT
ENST00000367942.3:c.484+169_484+170insACT	ENSP00000356919.3:n.484+169_484+170insACT
NM_007348.3:c.484+169_484+170insACT	NP_031374.2:n.484+169_484+170insACT
XM_006711224.1:c.484+169_484+170insACT	XP_006711287.1:n.484+169_484+170insACT
XM_011509308.1:c.484+169_484+170insACT	XP_011507610.1:n.484+169_484+170insACT
XM_011509309.1:c.484+169_484+170insACT	XP_011507611.1:n.484+169_484+170insACT
XM_011509310.1:c.484+169_484+170insACT	XP_011507612.1:n.484+169_484+170insACT
XM_011509310.2:c.484+169_484+170insACT	XP_011507612.1:n.484+169_484+170insACT
NM_007348.4:c.484+169_484+170insACT MANE Select	NP_031374.2:n.484+169_484+170insACT