Canonical Allele Identifier: CA343386307

Gene: ATF6

Linked Data

• gnomAD v4: 1-161791535-C-T
• MyVariant Identifiers: chr1:g.161761325C>T (hg19) ; chr1:g.161791535C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161791535C>T , CM000663.2:g.161791535C>T	GRCh38
NC_000001.10:g.161761325C>T , CM000663.1:g.161761325C>T	GRCh37
NC_000001.9:g.160027949C>T	NCBI36
NG_029773.1:g.30292C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.482C>T MANE Select	ENSP00000356919.3:p.Thr161Ile
ENST00000679833.1:c.482C>T	ENSP00000505321.1:p.Thr161Ile
ENST00000679853.1:c.482C>T	ENSP00000506149.1:p.Thr161Ile
ENST00000679886.1:c.83-10517C>T	ENSP00000506559.1:n.83-10517C>T
ENST00000680180.1:n.522C>T
ENST00000680462.1:c.482C>T	ENSP00000505583.1:p.Thr161Ile
ENST00000680481.1:c.*105C>T	ENSP00000505919.1:n.*105C>T
ENST00000680633.1:c.284C>T	ENSP00000505371.1:p.Thr95Ile
ENST00000680688.1:c.482C>T	ENSP00000504865.1:p.Thr161Ile
ENST00000681001.1:c.*334C>T	ENSP00000506145.1:n.*334C>T
ENST00000681036.1:c.284C>T	ENSP00000505474.1:p.Thr95Ile
ENST00000681169.1:c.482C>T	ENSP00000505455.1:p.Thr161Ile
ENST00000681187.1:n.522C>T
ENST00000681492.1:c.482C>T	ENSP00000506139.1:p.Thr161Ile
ENST00000681541.1:c.284C>T	ENSP00000506087.1:p.Thr95Ile
ENST00000681557.1:c.*283C>T	ENSP00000506229.1:n.*283C>T
ENST00000681738.1:c.482C>T	ENSP00000505025.1:p.Thr161Ile
ENST00000681779.1:n.532C>T
ENST00000681801.1:c.482C>T	ENSP00000505998.1:p.Thr161Ile
ENST00000681912.1:c.98C>T	ENSP00000505875.1:p.Thr33Ile
ENST00000367942.3:c.482C>T	ENSP00000356919.3:p.Thr161Ile
NM_007348.3:c.482C>T	NP_031374.2:p.Thr161Ile
XM_006711224.1:c.482C>T	XP_006711287.1:p.Thr161Ile
XM_011509308.1:c.482C>T	XP_011507610.1:p.Thr161Ile
XM_011509309.1:c.482C>T	XP_011507611.1:p.Thr161Ile
XM_011509310.1:c.482C>T	XP_011507612.1:p.Thr161Ile
XM_011509310.2:c.482C>T	XP_011507612.1:p.Thr161Ile
NM_007348.4:c.482C>T MANE Select	NP_031374.2:p.Thr161Ile