Canonical Allele Identifier: CA2563066416

Gene: ATF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161781920_161781921insACTCTAAGTCAGTC , CM000663.2:g.161781920_161781921insACTCTAAGTCAGTC	GRCh38
NC_000001.10:g.161751710_161751711insACTCTAAGTCAGTC , CM000663.1:g.161751710_161751711insACTCTAAGTCAGTC	GRCh37
NC_000001.9:g.160018334_160018335insACTCTAAGTCAGTC	NCBI36
NG_029773.1:g.20677_20678insACTCTAAGTCAGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.168_169insACTCTAAGTCAGTC MANE Select	ENSP00000356919.3:p.Phe57ThrfsTer15
ENST00000679833.1:c.168_169insACTCTAAGTCAGTC	ENSP00000505321.1:p.Phe57ThrfsTer15
ENST00000679853.1:c.168_169insACTCTAAGTCAGTC	ENSP00000506149.1:p.Phe57ThrfsTer15
ENST00000679886.1:c.82+15478_82+15479insACTCTAAGTCAGTC	ENSP00000506559.1:n.82+15478_82+15479insACTCTAAGTCAGTC
ENST00000680180.1:n.208_209insACTCTAAGTCAGTC
ENST00000680462.1:c.168_169insACTCTAAGTCAGTC	ENSP00000505583.1:p.Phe57ThrfsTer15
ENST00000680481.1:c.168_169insACTCTAAGTCAGTC	ENSP00000505919.1:p.Phe57ThrfsTer15
ENST00000680633.1:c.-31_-30insACTCTAAGTCAGTC	ENSP00000505371.1:n.-31_-30insACTCTAAGTCAGTC
ENST00000680688.1:c.168_169insACTCTAAGTCAGTC	ENSP00000504865.1:p.Phe57ThrfsTer15
ENST00000681001.1:c.*20_*21insACTCTAAGTCAGTC	ENSP00000506145.1:n.*20_*21insACTCTAAGTCAGTC
ENST00000681036.1:c.-31_-30insACTCTAAGTCAGTC	ENSP00000505474.1:n.-31_-30insACTCTAAGTCAGTC
ENST00000681169.1:c.168_169insACTCTAAGTCAGTC	ENSP00000505455.1:p.Phe57ThrfsTer15
ENST00000681187.1:n.208_209insACTCTAAGTCAGTC
ENST00000681492.1:c.168_169insACTCTAAGTCAGTC	ENSP00000506139.1:p.Phe57ThrfsTer15
ENST00000681541.1:c.-31_-30insACTCTAAGTCAGTC	ENSP00000506087.1:n.-31_-30insACTCTAAGTCAGTC
ENST00000681557.1:c.164_165insACTCTAAGTCAGTC	ENSP00000506229.1:p.Ile57Ter
ENST00000681738.1:c.168_169insACTCTAAGTCAGTC	ENSP00000505025.1:p.Phe57ThrfsTer15
ENST00000681779.1:n.218_219insACTCTAAGTCAGTC
ENST00000681801.1:c.168_169insACTCTAAGTCAGTC	ENSP00000505998.1:p.Phe57ThrfsTer15
ENST00000681912.1:c.-30-9488_-30-9487insACTCTAAGTCAGTC	ENSP00000505875.1:n.-30-9488_-30-9487insACTCTAAGTCAGTC
ENST00000367942.3:c.168_169insACTCTAAGTCAGTC	ENSP00000356919.3:p.Phe57ThrfsTer15
NM_007348.3:c.168_169insACTCTAAGTCAGTC	NP_031374.2:p.Phe57ThrfsTer15
XM_006711224.1:c.168_169insACTCTAAGTCAGTC	XP_006711287.1:p.Phe57ThrfsTer15
XM_011509308.1:c.168_169insACTCTAAGTCAGTC	XP_011507610.1:p.Phe57ThrfsTer15
XM_011509309.1:c.168_169insACTCTAAGTCAGTC	XP_011507611.1:p.Phe57ThrfsTer15
XM_011509310.1:c.168_169insACTCTAAGTCAGTC	XP_011507612.1:p.Phe57ThrfsTer15
XM_011509310.2:c.168_169insACTCTAAGTCAGTC	XP_011507612.1:p.Phe57ThrfsTer15
NM_007348.4:c.168_169insACTCTAAGTCAGTC MANE Select	NP_031374.2:p.Phe57ThrfsTer15