Canonical Allele Identifier: CA16068380

Gene: ATF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161945711G>A , CM000663.2:g.161945711G>A	GRCh38
NC_000001.10:g.161915501G>A , CM000663.1:g.161915501G>A	GRCh37
NC_000001.9:g.160182125G>A	NCBI36
NG_029773.1:g.184468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1805-12735G>A MANE Select	ENSP00000356919.3:n.1805-12735G>A
ENST00000679853.1:c.1802-12735G>A	ENSP00000506149.1:n.1802-12735G>A
ENST00000679886.1:c.1199-12735G>A	ENSP00000506559.1:n.1199-12735G>A
ENST00000680481.1:c.*1515-12735G>A	ENSP00000505919.1:n.*1515-12735G>A
ENST00000680688.1:c.1862-12735G>A	ENSP00000504865.1:n.1862-12735G>A
ENST00000681001.1:c.*1657-12735G>A	ENSP00000506145.1:n.*1657-12735G>A
ENST00000681036.1:c.1607-12735G>A	ENSP00000505474.1:n.1607-12735G>A
ENST00000681169.1:c.*723-12735G>A	ENSP00000505455.1:n.*723-12735G>A
ENST00000681492.1:c.1895-12735G>A	ENSP00000506139.1:n.1895-12735G>A
ENST00000681541.1:c.1607-12735G>A	ENSP00000506087.1:n.1607-12735G>A
ENST00000681557.1:c.*1606-12735G>A	ENSP00000506229.1:n.*1606-12735G>A
ENST00000681738.1:c.1805-12735G>A	ENSP00000505025.1:n.1805-12735G>A
ENST00000681801.1:c.1805-12735G>A	ENSP00000505998.1:n.1805-12735G>A
ENST00000681912.1:c.1421-12735G>A	ENSP00000505875.1:n.1421-12735G>A
ENST00000367942.3:c.1805-12735G>A	ENSP00000356919.3:n.1805-12735G>A
NM_007348.3:c.1805-12735G>A	NP_031374.2:n.1805-12735G>A
XM_006711224.1:c.1802-12735G>A	XP_006711287.1:n.1802-12735G>A
XM_011509308.1:c.1862-12735G>A	XP_011507610.1:n.1862-12735G>A
XM_011509309.1:c.1859-12735G>A	XP_011507611.1:n.1859-12735G>A
NM_007348.4:c.1805-12735G>A MANE Select	NP_031374.2:n.1805-12735G>A