Canonical Allele Identifier: CA2322494279
Gene: CDKN2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568576G= , CM000681.2:g.10568576G= GRCh38
NC_000019.9:g.10679252G= , CM000681.1:g.10679252G= GRCh37
NC_000019.8:g.10540252G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.78C= MANE Select ENSP00000377224.1:p.Arg26=
ENST00000335766.2:c.78C= ENSP00000337056.1:p.Arg26=
ENST00000393599.2:c.78C= ENSP00000377224.1:p.Arg26=
NM_001800.3:c.78C= NP_001791.1:p.Arg26=
NM_079421.2:c.78C= NP_524145.1:p.Arg26=
NM_001800.4:c.78C= MANE Select NP_001791.1:p.Arg26=
NM_079421.3:c.78C= NP_524145.1:p.Arg26=