Canonical Allele Identifier: CA343384363

Gene: ATF6

Linked Data

• MyVariant Identifiers: chr1:g.161751711T>G (hg19) ; chr1:g.161781921T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161781921T>G , CM000663.2:g.161781921T>G	GRCh38
NC_000001.10:g.161751711T>G , CM000663.1:g.161751711T>G	GRCh37
NC_000001.9:g.160018335T>G	NCBI36
NG_029773.1:g.20678T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.169T>G MANE Select	ENSP00000356919.3:p.Phe57Val
ENST00000679833.1:c.169T>G	ENSP00000505321.1:p.Phe57Val
ENST00000679853.1:c.169T>G	ENSP00000506149.1:p.Phe57Val
ENST00000679886.1:c.82+15479T>G	ENSP00000506559.1:n.82+15479T>G
ENST00000680180.1:n.209T>G
ENST00000680462.1:c.169T>G	ENSP00000505583.1:p.Phe57Val
ENST00000680481.1:c.169T>G	ENSP00000505919.1:p.Phe57Val
ENST00000680633.1:c.-30T>G	ENSP00000505371.1:n.-30T>G
ENST00000680688.1:c.169T>G	ENSP00000504865.1:p.Phe57Val
ENST00000681001.1:c.*21T>G	ENSP00000506145.1:n.*21T>G
ENST00000681036.1:c.-30T>G	ENSP00000505474.1:n.-30T>G
ENST00000681169.1:c.169T>G	ENSP00000505455.1:p.Phe57Val
ENST00000681187.1:n.209T>G
ENST00000681492.1:c.169T>G	ENSP00000506139.1:p.Phe57Val
ENST00000681541.1:c.-30T>G	ENSP00000506087.1:n.-30T>G
ENST00000681557.1:c.165T>G	ENSP00000506229.1:p.Ile55Met
ENST00000681738.1:c.169T>G	ENSP00000505025.1:p.Phe57Val
ENST00000681779.1:n.219T>G
ENST00000681801.1:c.169T>G	ENSP00000505998.1:p.Phe57Val
ENST00000681912.1:c.-30-9487T>G	ENSP00000505875.1:n.-30-9487T>G
ENST00000367942.3:c.169T>G	ENSP00000356919.3:p.Phe57Val
NM_007348.3:c.169T>G	NP_031374.2:p.Phe57Val
XM_006711224.1:c.169T>G	XP_006711287.1:p.Phe57Val
XM_011509308.1:c.169T>G	XP_011507610.1:p.Phe57Val
XM_011509309.1:c.169T>G	XP_011507611.1:p.Phe57Val
XM_011509310.1:c.169T>G	XP_011507612.1:p.Phe57Val
XM_011509310.2:c.169T>G	XP_011507612.1:p.Phe57Val
NM_007348.4:c.169T>G MANE Select	NP_031374.2:p.Phe57Val