Canonical Allele Identifier: CA343384389
Gene: ATF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161781931T>C , CM000663.2:g.161781931T>C GRCh38
NC_000001.10:g.161751721T>C , CM000663.1:g.161751721T>C GRCh37
NC_000001.9:g.160018345T>C NCBI36
NG_029773.1:g.20688T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367942.4:c.179T>C MANE Select ENSP00000356919.3:p.Leu60Pro
ENST00000679833.1:c.179T>C ENSP00000505321.1:p.Leu60Pro
ENST00000679853.1:c.179T>C ENSP00000506149.1:p.Leu60Pro
ENST00000679886.1:c.82+15489T>C ENSP00000506559.1:n.82+15489T>C
ENST00000680180.1:n.219T>C
ENST00000680462.1:c.179T>C ENSP00000505583.1:p.Leu60Pro
ENST00000680481.1:c.179T>C ENSP00000505919.1:p.Leu60Pro
ENST00000680633.1:c.-20T>C ENSP00000505371.1:n.-20T>C
ENST00000680688.1:c.179T>C ENSP00000504865.1:p.Leu60Pro
ENST00000681001.1:c.*31T>C ENSP00000506145.1:n.*31T>C
ENST00000681036.1:c.-20T>C ENSP00000505474.1:n.-20T>C
ENST00000681169.1:c.179T>C ENSP00000505455.1:p.Leu60Pro
ENST00000681187.1:n.219T>C
ENST00000681492.1:c.179T>C ENSP00000506139.1:p.Leu60Pro
ENST00000681541.1:c.-20T>C ENSP00000506087.1:n.-20T>C
ENST00000681557.1:c.175T>C ENSP00000506229.1:p.Leu59=
ENST00000681738.1:c.179T>C ENSP00000505025.1:p.Leu60Pro
ENST00000681779.1:n.229T>C
ENST00000681801.1:c.179T>C ENSP00000505998.1:p.Leu60Pro
ENST00000681912.1:c.-30-9477T>C ENSP00000505875.1:n.-30-9477T>C
ENST00000367942.3:c.179T>C ENSP00000356919.3:p.Leu60Pro
NM_007348.3:c.179T>C NP_031374.2:p.Leu60Pro
XM_006711224.1:c.179T>C XP_006711287.1:p.Leu60Pro
XM_011509308.1:c.179T>C XP_011507610.1:p.Leu60Pro
XM_011509309.1:c.179T>C XP_011507611.1:p.Leu60Pro
XM_011509310.1:c.179T>C XP_011507612.1:p.Leu60Pro
XM_011509310.2:c.179T>C XP_011507612.1:p.Leu60Pro
NM_007348.4:c.179T>C MANE Select NP_031374.2:p.Leu60Pro