Canonical Allele Identifier: CA343380936

Gene: ATF6

Linked Data

• MyVariant Identifiers: chr1:g.161823040T>C (hg19) ; chr1:g.161853250T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853250T>C , CM000663.2:g.161853250T>C	GRCh38
NC_000001.10:g.161823040T>C , CM000663.1:g.161823040T>C	GRCh37
NC_000001.9:g.160089664T>C	NCBI36
NG_029773.1:g.92007T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1460T>C MANE Select	ENSP00000356919.3:p.Val487Ala
ENST00000679833.1:c.1460T>C	ENSP00000505321.1:p.Val487Ala
ENST00000679853.1:c.1460T>C	ENSP00000506149.1:p.Val487Ala
ENST00000679886.1:c.854T>C	ENSP00000506559.1:p.Val285Ala
ENST00000680180.1:n.1500T>C
ENST00000680462.1:c.1460T>C	ENSP00000505583.1:p.Val487Ala
ENST00000680481.1:c.*1083T>C	ENSP00000505919.1:n.*1083T>C
ENST00000680688.1:c.1517T>C	ENSP00000504865.1:p.Val506Ala
ENST00000681001.1:c.*1312T>C	ENSP00000506145.1:n.*1312T>C
ENST00000681036.1:c.1262T>C	ENSP00000505474.1:p.Val421Ala
ENST00000681169.1:c.*378T>C	ENSP00000505455.1:n.*378T>C
ENST00000681187.1:n.1500T>C
ENST00000681492.1:c.1460T>C	ENSP00000506139.1:p.Val487Ala
ENST00000681541.1:c.1262T>C	ENSP00000506087.1:p.Val421Ala
ENST00000681557.1:c.*1261T>C	ENSP00000506229.1:n.*1261T>C
ENST00000681738.1:c.1460T>C	ENSP00000505025.1:p.Val487Ala
ENST00000681779.1:n.1510T>C
ENST00000681801.1:c.1460T>C	ENSP00000505998.1:p.Val487Ala
ENST00000681912.1:c.1076T>C	ENSP00000505875.1:p.Val359Ala
ENST00000367942.3:c.1460T>C	ENSP00000356919.3:p.Val487Ala
ENST00000476437.1:n.667T>C
NM_007348.3:c.1460T>C	NP_031374.2:p.Val487Ala
XM_006711224.1:c.1460T>C	XP_006711287.1:p.Val487Ala
XM_011509308.1:c.1517T>C	XP_011507610.1:p.Val506Ala
XM_011509309.1:c.1517T>C	XP_011507611.1:p.Val506Ala
XM_011509310.1:c.1517T>C	XP_011507612.1:p.Val506Ala
XM_011509310.2:c.1517T>C	XP_011507612.1:p.Val506Ala
NM_007348.4:c.1460T>C MANE Select	NP_031374.2:p.Val487Ala