Canonical Allele Identifier: CA343380926

Gene: ATF6

Linked Data

• MyVariant Identifiers: chr1:g.161823038G>C (hg19) ; chr1:g.161853248G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853248G>C , CM000663.2:g.161853248G>C	GRCh38
NC_000001.10:g.161823038G>C , CM000663.1:g.161823038G>C	GRCh37
NC_000001.9:g.160089662G>C	NCBI36
NG_029773.1:g.92005G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1458G>C MANE Select	ENSP00000356919.3:p.Trp486Cys
ENST00000679833.1:c.1458G>C	ENSP00000505321.1:p.Trp486Cys
ENST00000679853.1:c.1458G>C	ENSP00000506149.1:p.Trp486Cys
ENST00000679886.1:c.852G>C	ENSP00000506559.1:p.Trp284Cys
ENST00000680180.1:n.1498G>C
ENST00000680462.1:c.1458G>C	ENSP00000505583.1:p.Trp486Cys
ENST00000680481.1:c.*1081G>C	ENSP00000505919.1:n.*1081G>C
ENST00000680688.1:c.1515G>C	ENSP00000504865.1:p.Trp505Cys
ENST00000681001.1:c.*1310G>C	ENSP00000506145.1:n.*1310G>C
ENST00000681036.1:c.1260G>C	ENSP00000505474.1:p.Trp420Cys
ENST00000681169.1:c.*376G>C	ENSP00000505455.1:n.*376G>C
ENST00000681187.1:n.1498G>C
ENST00000681492.1:c.1458G>C	ENSP00000506139.1:p.Trp486Cys
ENST00000681541.1:c.1260G>C	ENSP00000506087.1:p.Trp420Cys
ENST00000681557.1:c.*1259G>C	ENSP00000506229.1:n.*1259G>C
ENST00000681738.1:c.1458G>C	ENSP00000505025.1:p.Trp486Cys
ENST00000681779.1:n.1508G>C
ENST00000681801.1:c.1458G>C	ENSP00000505998.1:p.Trp486Cys
ENST00000681912.1:c.1074G>C	ENSP00000505875.1:p.Trp358Cys
ENST00000367942.3:c.1458G>C	ENSP00000356919.3:p.Trp486Cys
ENST00000476437.1:n.665G>C
NM_007348.3:c.1458G>C	NP_031374.2:p.Trp486Cys
XM_006711224.1:c.1458G>C	XP_006711287.1:p.Trp486Cys
XM_011509308.1:c.1515G>C	XP_011507610.1:p.Trp505Cys
XM_011509309.1:c.1515G>C	XP_011507611.1:p.Trp505Cys
XM_011509310.1:c.1515G>C	XP_011507612.1:p.Trp505Cys
XM_011509310.2:c.1515G>C	XP_011507612.1:p.Trp505Cys
NM_007348.4:c.1458G>C MANE Select	NP_031374.2:p.Trp486Cys