Canonical Allele Identifier: CA343380940

Gene: ATF6

Linked Data

• MyVariant Identifiers: chr1:g.161823042C>G (hg19) ; chr1:g.161853252C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853252C>G , CM000663.2:g.161853252C>G	GRCh38
NC_000001.10:g.161823042C>G , CM000663.1:g.161823042C>G	GRCh37
NC_000001.9:g.160089666C>G	NCBI36
NG_029773.1:g.92009C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1462C>G MANE Select	ENSP00000356919.3:p.His488Asp
ENST00000679833.1:c.1462C>G	ENSP00000505321.1:p.His488Asp
ENST00000679853.1:c.1462C>G	ENSP00000506149.1:p.His488Asp
ENST00000679886.1:c.856C>G	ENSP00000506559.1:p.His286Asp
ENST00000680180.1:n.1502C>G
ENST00000680462.1:c.1462C>G	ENSP00000505583.1:p.His488Asp
ENST00000680481.1:c.*1085C>G	ENSP00000505919.1:n.*1085C>G
ENST00000680688.1:c.1519C>G	ENSP00000504865.1:p.His507Asp
ENST00000681001.1:c.*1314C>G	ENSP00000506145.1:n.*1314C>G
ENST00000681036.1:c.1264C>G	ENSP00000505474.1:p.His422Asp
ENST00000681169.1:c.*380C>G	ENSP00000505455.1:n.*380C>G
ENST00000681187.1:n.1502C>G
ENST00000681492.1:c.1462C>G	ENSP00000506139.1:p.His488Asp
ENST00000681541.1:c.1264C>G	ENSP00000506087.1:p.His422Asp
ENST00000681557.1:c.*1263C>G	ENSP00000506229.1:n.*1263C>G
ENST00000681738.1:c.1462C>G	ENSP00000505025.1:p.His488Asp
ENST00000681779.1:n.1512C>G
ENST00000681801.1:c.1462C>G	ENSP00000505998.1:p.His488Asp
ENST00000681912.1:c.1078C>G	ENSP00000505875.1:p.His360Asp
ENST00000367942.3:c.1462C>G	ENSP00000356919.3:p.His488Asp
ENST00000476437.1:n.669C>G
NM_007348.3:c.1462C>G	NP_031374.2:p.His488Asp
XM_006711224.1:c.1462C>G	XP_006711287.1:p.His488Asp
XM_011509308.1:c.1519C>G	XP_011507610.1:p.His507Asp
XM_011509309.1:c.1519C>G	XP_011507611.1:p.His507Asp
XM_011509310.1:c.1519C>G	XP_011507612.1:p.His507Asp
XM_011509310.2:c.1519C>G	XP_011507612.1:p.His507Asp
NM_007348.4:c.1462C>G MANE Select	NP_031374.2:p.His488Asp