Canonical Allele Identifier: CA404021586
Gene: CDKN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568575G>C , CM000681.2:g.10568575G>C GRCh38
NC_000019.9:g.10679251G>C , CM000681.1:g.10679251G>C GRCh37
NC_000019.8:g.10540251G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.79C>G MANE Select ENSP00000377224.1:p.Leu27Val
ENST00000335766.2:c.79C>G ENSP00000337056.1:p.Leu27Val
ENST00000393599.2:c.79C>G ENSP00000377224.1:p.Leu27Val
NM_001800.3:c.79C>G NP_001791.1:p.Leu27Val
NM_079421.2:c.79C>G NP_524145.1:p.Leu27Val
NM_001800.4:c.79C>G MANE Select NP_001791.1:p.Leu27Val
NM_079421.3:c.79C>G NP_524145.1:p.Leu27Val