Canonical Allele Identifier: CA2063464887

Gene: ALDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111807875_111807879delinsATTTT , CM000674.2:g.111807875_111807879delinsATTTT	GRCh38
NC_000012.11:g.112245679_112245683delinsATTTT , CM000674.1:g.112245679_112245683delinsATTTT	GRCh37
NC_000012.10:g.110730062_110730066delinsATTTT	NCBI36
NG_012250.1:g.46334_46338delinsATTTT
NG_012250.2:g.45989_45993delinsATTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261733.7:c.1522-1668_1522-1664delinsATTTT MANE Select	ENSP00000261733.2:n.1522-1668_1522-1664delinsATTTT
ENST00000261733.6:c.1522-1668_1522-1664delinsATTTT	ENSP00000261733.2:n.1522-1668_1522-1664delinsATTTT
ENST00000416293.7:c.1381-1668_1381-1664delinsATTTT	ENSP00000403349.3:n.1381-1668_1381-1664delinsATTTT
ENST00000548536.1:c.*1398-1668_*1398-1664delinsATTTT	ENSP00000448179.1:n.*1398-1668_*1398-1664delinsATTTT
ENST00000549106.1:c.453-1668_453-1664delinsATTTT
NM_000690.3:c.1522-1668_1522-1664delinsATTTT	NP_000681.2:n.1522-1668_1522-1664delinsATTTT
NM_001204889.1:c.1381-1668_1381-1664delinsATTTT	NP_001191818.1:n.1381-1668_1381-1664delinsATTTT
NM_000690.4:c.1522-1668_1522-1664delinsATTTT MANE Select	NP_000681.2:n.1522-1668_1522-1664delinsATTTT
NM_001204889.2:c.1381-1668_1381-1664delinsATTTT	NP_001191818.1:n.1381-1668_1381-1664delinsATTTT