Canonical Allele Identifier: CA343380953

Gene: ATF6

Linked Data

• MyVariant Identifiers: chr1:g.161823046G>T (hg19) ; chr1:g.161853256G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853256G>T , CM000663.2:g.161853256G>T	GRCh38
NC_000001.10:g.161823046G>T , CM000663.1:g.161823046G>T	GRCh37
NC_000001.9:g.160089670G>T	NCBI36
NG_029773.1:g.92013G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1466G>T MANE Select	ENSP00000356919.3:p.Arg489Ile
ENST00000679833.1:c.1466G>T	ENSP00000505321.1:p.Arg489Ile
ENST00000679853.1:c.1466G>T	ENSP00000506149.1:p.Arg489Ile
ENST00000679886.1:c.860G>T	ENSP00000506559.1:p.Arg287Ile
ENST00000680180.1:n.1506G>T
ENST00000680462.1:c.1466G>T	ENSP00000505583.1:p.Arg489Ile
ENST00000680481.1:c.*1089G>T	ENSP00000505919.1:n.*1089G>T
ENST00000680688.1:c.1523G>T	ENSP00000504865.1:p.Arg508Ile
ENST00000681001.1:c.*1318G>T	ENSP00000506145.1:n.*1318G>T
ENST00000681036.1:c.1268G>T	ENSP00000505474.1:p.Arg423Ile
ENST00000681169.1:c.*384G>T	ENSP00000505455.1:n.*384G>T
ENST00000681187.1:n.1506G>T
ENST00000681492.1:c.1466G>T	ENSP00000506139.1:p.Arg489Ile
ENST00000681541.1:c.1268G>T	ENSP00000506087.1:p.Arg423Ile
ENST00000681557.1:c.*1267G>T	ENSP00000506229.1:n.*1267G>T
ENST00000681738.1:c.1466G>T	ENSP00000505025.1:p.Arg489Ile
ENST00000681779.1:n.1516G>T
ENST00000681801.1:c.1466G>T	ENSP00000505998.1:p.Arg489Ile
ENST00000681912.1:c.1082G>T	ENSP00000505875.1:p.Arg361Ile
ENST00000367942.3:c.1466G>T	ENSP00000356919.3:p.Arg489Ile
ENST00000476437.1:n.673G>T
NM_007348.3:c.1466G>T	NP_031374.2:p.Arg489Ile
XM_006711224.1:c.1466G>T	XP_006711287.1:p.Arg489Ile
XM_011509308.1:c.1523G>T	XP_011507610.1:p.Arg508Ile
XM_011509309.1:c.1523G>T	XP_011507611.1:p.Arg508Ile
XM_011509310.1:c.1523G>T	XP_011507612.1:p.Arg508Ile
XM_011509310.2:c.1523G>T	XP_011507612.1:p.Arg508Ile
NM_007348.4:c.1466G>T MANE Select	NP_031374.2:p.Arg489Ile