Canonical Allele Identifier: CA343380549

Gene: ATF6

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161851739C>G , CM000663.2:g.161851739C>G	GRCh38
NC_000001.10:g.161821529C>G , CM000663.1:g.161821529C>G	GRCh37
NC_000001.9:g.160088153C>G	NCBI36
NG_029773.1:g.90496C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1337C>G MANE Select	ENSP00000356919.3:p.Ser446Ter
ENST00000679833.1:c.1337C>G	ENSP00000505321.1:p.Ser446Ter
ENST00000679853.1:c.1337C>G	ENSP00000506149.1:p.Ser446Ter
ENST00000679886.1:c.731C>G	ENSP00000506559.1:p.Ser244Ter
ENST00000680180.1:n.1377C>G
ENST00000680462.1:c.1337C>G	ENSP00000505583.1:p.Ser446Ter
ENST00000680481.1:c.*960C>G	ENSP00000505919.1:n.*960C>G
ENST00000680688.1:c.1394C>G	ENSP00000504865.1:p.Ser465Ter
ENST00000681001.1:c.*1189C>G	ENSP00000506145.1:n.*1189C>G
ENST00000681036.1:c.1139C>G	ENSP00000505474.1:p.Ser380Ter
ENST00000681169.1:c.*255C>G	ENSP00000505455.1:n.*255C>G
ENST00000681187.1:n.1377C>G
ENST00000681492.1:c.1337C>G	ENSP00000506139.1:p.Ser446Ter
ENST00000681541.1:c.1139C>G	ENSP00000506087.1:p.Ser380Ter
ENST00000681557.1:c.*1138C>G	ENSP00000506229.1:n.*1138C>G
ENST00000681738.1:c.1337C>G	ENSP00000505025.1:p.Ser446Ter
ENST00000681779.1:n.1387C>G
ENST00000681801.1:c.1337C>G	ENSP00000505998.1:p.Ser446Ter
ENST00000681912.1:c.953C>G	ENSP00000505875.1:p.Ser318Ter
ENST00000367942.3:c.1337C>G	ENSP00000356919.3:p.Ser446Ter
ENST00000476437.1:n.544C>G
NM_007348.3:c.1337C>G	NP_031374.2:p.Ser446Ter
XM_006711224.1:c.1337C>G	XP_006711287.1:p.Ser446Ter
XM_011509308.1:c.1394C>G	XP_011507610.1:p.Ser465Ter
XM_011509309.1:c.1394C>G	XP_011507611.1:p.Ser465Ter
XM_011509310.1:c.1394C>G	XP_011507612.1:p.Ser465Ter
XM_011509310.2:c.1394C>G	XP_011507612.1:p.Ser465Ter
NM_007348.4:c.1337C>G MANE Select	NP_031374.2:p.Ser446Ter