Canonical Allele Identifier: CA2648814390

Gene: ATF6

Linked Data

• gnomAD v4: 1-161853274-C-CCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853275_161853277dup , CM000663.2:g.161853275_161853277dup	GRCh38
NC_000001.10:g.161823065_161823067dup , CM000663.1:g.161823065_161823067dup	GRCh37
NC_000001.9:g.160089689_160089691dup	NCBI36
NG_029773.1:g.92032_92034dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1485_1487dup MANE Select	ENSP00000356919.3:p.Thr495_Lys496insAsn
ENST00000679833.1:c.1485_1487dup	ENSP00000505321.1:p.Thr495_Lys496insAsn
ENST00000679853.1:c.1485_1487dup	ENSP00000506149.1:p.Thr495_Lys496insAsn
ENST00000679886.1:c.879_881dup	ENSP00000506559.1:p.Thr293_Lys294insAsn
ENST00000680180.1:n.1525_1527dup
ENST00000680462.1:c.1485_1487dup	ENSP00000505583.1:p.Thr495_Lys496insAsn
ENST00000680481.1:c.*1108_*1110dup	ENSP00000505919.1:n.*1108_*1110dup
ENST00000680688.1:c.1542_1544dup	ENSP00000504865.1:p.Thr514_Lys515insAsn
ENST00000681001.1:c.*1337_*1339dup	ENSP00000506145.1:n.*1337_*1339dup
ENST00000681036.1:c.1287_1289dup	ENSP00000505474.1:p.Thr429_Lys430insAsn
ENST00000681169.1:c.*403_*405dup	ENSP00000505455.1:n.*403_*405dup
ENST00000681187.1:n.1525_1527dup
ENST00000681492.1:c.1485_1487dup	ENSP00000506139.1:p.Thr495_Lys496insAsn
ENST00000681541.1:c.1287_1289dup	ENSP00000506087.1:p.Thr429_Lys430insAsn
ENST00000681557.1:c.*1286_*1288dup	ENSP00000506229.1:n.*1286_*1288dup
ENST00000681738.1:c.1485_1487dup	ENSP00000505025.1:p.Thr495_Lys496insAsn
ENST00000681779.1:n.1535_1537dup
ENST00000681801.1:c.1485_1487dup	ENSP00000505998.1:p.Thr495_Lys496insAsn
ENST00000681912.1:c.1101_1103dup	ENSP00000505875.1:p.Thr367_Lys368insAsn
ENST00000367942.3:c.1485_1487dup	ENSP00000356919.3:p.Thr495_Lys496insAsn
ENST00000476437.1:n.692_694dup
NM_007348.3:c.1485_1487dup	NP_031374.2:p.Thr495_Lys496insAsn
XM_006711224.1:c.1485_1487dup	XP_006711287.1:p.Thr495_Lys496insAsn
XM_011509308.1:c.1542_1544dup	XP_011507610.1:p.Thr514_Lys515insAsn
XM_011509309.1:c.1542_1544dup	XP_011507611.1:p.Thr514_Lys515insAsn
XM_011509310.1:c.1542_1544dup	XP_011507612.1:p.Thr514_Lys515insAsn
XM_011509310.2:c.1542_1544dup	XP_011507612.1:p.Thr514_Lys515insAsn
NM_007348.4:c.1485_1487dup MANE Select	NP_031374.2:p.Thr495_Lys496insAsn