Canonical Allele Identifier: CA2746385239

Gene: ATF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161782009_161782010insACG , CM000663.2:g.161782009_161782010insACG	GRCh38
NC_000001.10:g.161751799_161751800insACG , CM000663.1:g.161751799_161751800insACG	GRCh37
NC_000001.9:g.160018423_160018424insACG	NCBI36
NG_029773.1:g.20766_20767insACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.247+10_247+11insACG MANE Select	ENSP00000356919.3:n.247+10_247+11insACG
ENST00000679833.1:c.247+10_247+11insACG	ENSP00000505321.1:n.247+10_247+11insACG
ENST00000679853.1:c.247+10_247+11insACG	ENSP00000506149.1:n.247+10_247+11insACG
ENST00000679886.1:c.82+15567_82+15568insACG	ENSP00000506559.1:n.82+15567_82+15568insACG
ENST00000680180.1:n.287+10_287+11insACG
ENST00000680462.1:c.247+10_247+11insACG	ENSP00000505583.1:n.247+10_247+11insACG
ENST00000680481.1:c.247+10_247+11insACG	ENSP00000505919.1:n.247+10_247+11insACG
ENST00000680633.1:c.49+10_49+11insACG	ENSP00000505371.1:n.49+10_49+11insACG
ENST00000680688.1:c.247+10_247+11insACG	ENSP00000504865.1:n.247+10_247+11insACG
ENST00000681001.1:c.*99+10_*99+11insACG	ENSP00000506145.1:n.*99+10_*99+11insACG
ENST00000681036.1:c.49+10_49+11insACG	ENSP00000505474.1:n.49+10_49+11insACG
ENST00000681169.1:c.247+10_247+11insACG	ENSP00000505455.1:n.247+10_247+11insACG
ENST00000681187.1:n.287+10_287+11insACG
ENST00000681492.1:c.247+10_247+11insACG	ENSP00000506139.1:n.247+10_247+11insACG
ENST00000681541.1:c.49+10_49+11insACG	ENSP00000506087.1:n.49+10_49+11insACG
ENST00000681557.1:c.*48+10_*48+11insACG	ENSP00000506229.1:n.*48+10_*48+11insACG
ENST00000681738.1:c.247+10_247+11insACG	ENSP00000505025.1:n.247+10_247+11insACG
ENST00000681779.1:n.297+10_297+11insACG
ENST00000681801.1:c.247+10_247+11insACG	ENSP00000505998.1:n.247+10_247+11insACG
ENST00000681912.1:c.-30-9399_-30-9398insACG	ENSP00000505875.1:n.-30-9399_-30-9398insACG
ENST00000367942.3:c.247+10_247+11insACG	ENSP00000356919.3:n.247+10_247+11insACG
NM_007348.3:c.247+10_247+11insACG	NP_031374.2:n.247+10_247+11insACG
XM_006711224.1:c.247+10_247+11insACG	XP_006711287.1:n.247+10_247+11insACG
XM_011509308.1:c.247+10_247+11insACG	XP_011507610.1:n.247+10_247+11insACG
XM_011509309.1:c.247+10_247+11insACG	XP_011507611.1:n.247+10_247+11insACG
XM_011509310.1:c.247+10_247+11insACG	XP_011507612.1:n.247+10_247+11insACG
XM_011509310.2:c.247+10_247+11insACG	XP_011507612.1:n.247+10_247+11insACG
NM_007348.4:c.247+10_247+11insACG MANE Select	NP_031374.2:n.247+10_247+11insACG