Canonical Allele Identifier: CA343380857
Gene: ATF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161853228A>T , CM000663.2:g.161853228A>T GRCh38
NC_000001.10:g.161823018A>T , CM000663.1:g.161823018A>T GRCh37
NC_000001.9:g.160089642A>T NCBI36
NG_029773.1:g.91985A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367942.4:c.1438A>T MANE Select ENSP00000356919.3:p.Asn480Tyr
ENST00000679833.1:c.1438A>T ENSP00000505321.1:p.Asn480Tyr
ENST00000679853.1:c.1438A>T ENSP00000506149.1:p.Asn480Tyr
ENST00000679886.1:c.832A>T ENSP00000506559.1:p.Asn278Tyr
ENST00000680180.1:n.1478A>T
ENST00000680462.1:c.1438A>T ENSP00000505583.1:p.Asn480Tyr
ENST00000680481.1:c.*1061A>T ENSP00000505919.1:n.*1061A>T
ENST00000680688.1:c.1495A>T ENSP00000504865.1:p.Asn499Tyr
ENST00000681001.1:c.*1290A>T ENSP00000506145.1:n.*1290A>T
ENST00000681036.1:c.1240A>T ENSP00000505474.1:p.Asn414Tyr
ENST00000681169.1:c.*356A>T ENSP00000505455.1:n.*356A>T
ENST00000681187.1:n.1478A>T
ENST00000681492.1:c.1438A>T ENSP00000506139.1:p.Asn480Tyr
ENST00000681541.1:c.1240A>T ENSP00000506087.1:p.Asn414Tyr
ENST00000681557.1:c.*1239A>T ENSP00000506229.1:n.*1239A>T
ENST00000681738.1:c.1438A>T ENSP00000505025.1:p.Asn480Tyr
ENST00000681779.1:n.1488A>T
ENST00000681801.1:c.1438A>T ENSP00000505998.1:p.Asn480Tyr
ENST00000681912.1:c.1054A>T ENSP00000505875.1:p.Asn352Tyr
ENST00000367942.3:c.1438A>T ENSP00000356919.3:p.Asn480Tyr
ENST00000476437.1:n.645A>T
NM_007348.3:c.1438A>T NP_031374.2:p.Asn480Tyr
XM_006711224.1:c.1438A>T XP_006711287.1:p.Asn480Tyr
XM_011509308.1:c.1495A>T XP_011507610.1:p.Asn499Tyr
XM_011509309.1:c.1495A>T XP_011507611.1:p.Asn499Tyr
XM_011509310.1:c.1495A>T XP_011507612.1:p.Asn499Tyr
XM_011509310.2:c.1495A>T XP_011507612.1:p.Asn499Tyr
NM_007348.4:c.1438A>T MANE Select NP_031374.2:p.Asn480Tyr