Canonical Allele Identifier: CA2746388160
Gene: ATF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161853191_161853192insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG , CM000663.2:g.161853191_161853192insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG GRCh38
NC_000001.10:g.161822981_161822982insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG , CM000663.1:g.161822981_161822982insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG GRCh37
NC_000001.9:g.160089605_160089606insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG NCBI36
NG_029773.1:g.91948_91949insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367942.4:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG MANE Select ENSP00000356919.3:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000679833.1:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000505321.1:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000679853.1:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000506149.1:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000679886.1:c.828-33_828-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000506559.1:n.828-33_828-32insGGGGGGGGGGGGGGGGGGGTGAGGG...
ENST00000680180.1:n.1474-33_1474-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG
ENST00000680462.1:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000505583.1:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000680481.1:c.*1057-33_*1057-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000505919.1:n.*1057-33_*1057-32insGGGGGGGGGGGGGGGGGGGTG...
ENST00000680688.1:c.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000504865.1:n.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000681001.1:c.*1286-33_*1286-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000506145.1:n.*1286-33_*1286-32insGGGGGGGGGGGGGGGGGGGTG...
ENST00000681036.1:c.1236-33_1236-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000505474.1:n.1236-33_1236-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000681169.1:c.*352-33_*352-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000505455.1:n.*352-33_*352-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000681187.1:n.1474-33_1474-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG
ENST00000681492.1:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000506139.1:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000681541.1:c.1236-33_1236-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000506087.1:n.1236-33_1236-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000681557.1:c.*1235-33_*1235-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000506229.1:n.*1235-33_*1235-32insGGGGGGGGGGGGGGGGGGGTG...
ENST00000681738.1:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000505025.1:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000681779.1:n.1484-33_1484-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG
ENST00000681801.1:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000505998.1:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000681912.1:c.1050-33_1050-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000505875.1:n.1050-33_1050-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000367942.3:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG ENSP00000356919.3:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAG...
ENST00000476437.1:n.641-33_641-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG
NM_007348.3:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG NP_031374.2:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG...
XM_006711224.1:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG XP_006711287.1:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGG...
XM_011509308.1:c.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG XP_011507610.1:n.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAGGGG...
XM_011509309.1:c.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG XP_011507611.1:n.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAGGGG...
XM_011509310.1:c.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG XP_011507612.1:n.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAGGGG...
XM_011509310.2:c.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG XP_011507612.1:n.1491-33_1491-32insGGGGGGGGGGGGGGGGGGGTGAGGGG...
NM_007348.4:c.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG MANE Select NP_031374.2:n.1434-33_1434-32insGGGGGGGGGGGGGGGGGGGTGAGGGGGGG...