Canonical Allele Identifier: CA2648814337

Gene: ATF6

Linked Data

• gnomAD v4: 1-161853173-T-TTAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853174_161853175insAAAT , CM000663.2:g.161853174_161853175insAAAT	GRCh38
NC_000001.10:g.161822964_161822965insAAAT , CM000663.1:g.161822964_161822965insAAAT	GRCh37
NC_000001.9:g.160089588_160089589insAAAT	NCBI36
NG_029773.1:g.91931_91932insAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1434-50_1434-49insAAAT MANE Select	ENSP00000356919.3:n.1434-50_1434-49insAAAT
ENST00000679833.1:c.1434-50_1434-49insAAAT	ENSP00000505321.1:n.1434-50_1434-49insAAAT
ENST00000679853.1:c.1434-50_1434-49insAAAT	ENSP00000506149.1:n.1434-50_1434-49insAAAT
ENST00000679886.1:c.828-50_828-49insAAAT	ENSP00000506559.1:n.828-50_828-49insAAAT
ENST00000680180.1:n.1474-50_1474-49insAAAT
ENST00000680462.1:c.1434-50_1434-49insAAAT	ENSP00000505583.1:n.1434-50_1434-49insAAAT
ENST00000680481.1:c.*1057-50_*1057-49insAAAT	ENSP00000505919.1:n.*1057-50_*1057-49insAAAT
ENST00000680688.1:c.1491-50_1491-49insAAAT	ENSP00000504865.1:n.1491-50_1491-49insAAAT
ENST00000681001.1:c.*1286-50_*1286-49insAAAT	ENSP00000506145.1:n.*1286-50_*1286-49insAAAT
ENST00000681036.1:c.1236-50_1236-49insAAAT	ENSP00000505474.1:n.1236-50_1236-49insAAAT
ENST00000681169.1:c.*352-50_*352-49insAAAT	ENSP00000505455.1:n.*352-50_*352-49insAAAT
ENST00000681187.1:n.1474-50_1474-49insAAAT
ENST00000681492.1:c.1434-50_1434-49insAAAT	ENSP00000506139.1:n.1434-50_1434-49insAAAT
ENST00000681541.1:c.1236-50_1236-49insAAAT	ENSP00000506087.1:n.1236-50_1236-49insAAAT
ENST00000681557.1:c.*1235-50_*1235-49insAAAT	ENSP00000506229.1:n.*1235-50_*1235-49insAAAT
ENST00000681738.1:c.1434-50_1434-49insAAAT	ENSP00000505025.1:n.1434-50_1434-49insAAAT
ENST00000681779.1:n.1484-50_1484-49insAAAT
ENST00000681801.1:c.1434-50_1434-49insAAAT	ENSP00000505998.1:n.1434-50_1434-49insAAAT
ENST00000681912.1:c.1050-50_1050-49insAAAT	ENSP00000505875.1:n.1050-50_1050-49insAAAT
ENST00000367942.3:c.1434-50_1434-49insAAAT	ENSP00000356919.3:n.1434-50_1434-49insAAAT
ENST00000476437.1:n.641-50_641-49insAAAT
NM_007348.3:c.1434-50_1434-49insAAAT	NP_031374.2:n.1434-50_1434-49insAAAT
XM_006711224.1:c.1434-50_1434-49insAAAT	XP_006711287.1:n.1434-50_1434-49insAAAT
XM_011509308.1:c.1491-50_1491-49insAAAT	XP_011507610.1:n.1491-50_1491-49insAAAT
XM_011509309.1:c.1491-50_1491-49insAAAT	XP_011507611.1:n.1491-50_1491-49insAAAT
XM_011509310.1:c.1491-50_1491-49insAAAT	XP_011507612.1:n.1491-50_1491-49insAAAT
XM_011509310.2:c.1491-50_1491-49insAAAT	XP_011507612.1:n.1491-50_1491-49insAAAT
NM_007348.4:c.1434-50_1434-49insAAAT MANE Select	NP_031374.2:n.1434-50_1434-49insAAAT