Canonical Allele Identifier: CA2322494176

Gene: CDKN2D

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10568392_10568393delinsAG , CM000681.2:g.10568392_10568393delinsAG	GRCh38
NC_000019.9:g.10679068_10679069delinsAG , CM000681.1:g.10679068_10679069delinsAG	GRCh37
NC_000019.8:g.10540068_10540069delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393599.3:c.141+120_141+121delinsCT MANE Select	ENSP00000377224.1:n.141+120_141+121delinsCT
ENST00000335766.2:c.141+120_141+121delinsCT	ENSP00000337056.1:n.141+120_141+121delinsCT
ENST00000393599.2:c.141+120_141+121delinsCT	ENSP00000377224.1:n.141+120_141+121delinsCT
NM_001800.3:c.141+120_141+121delinsCT	NP_001791.1:n.141+120_141+121delinsCT
NM_079421.2:c.141+120_141+121delinsCT	NP_524145.1:n.141+120_141+121delinsCT
NM_001800.4:c.141+120_141+121delinsCT MANE Select	NP_001791.1:n.141+120_141+121delinsCT
NM_079421.3:c.141+120_141+121delinsCT	NP_524145.1:n.141+120_141+121delinsCT