Canonical Allele Identifier: CA2582401915
Gene: CDKN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568386G>T , CM000681.2:g.10568386G>T GRCh38
NC_000019.9:g.10679062G>T , CM000681.1:g.10679062G>T GRCh37
NC_000019.8:g.10540062G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393599.3:c.141+127C>A MANE Select ENSP00000377224.1:n.141+127C>A
ENST00000335766.2:c.141+127C>A ENSP00000337056.1:n.141+127C>A
ENST00000393599.2:c.141+127C>A ENSP00000377224.1:n.141+127C>A
NM_001800.3:c.141+127C>A NP_001791.1:n.141+127C>A
NM_079421.2:c.141+127C>A NP_524145.1:n.141+127C>A
NM_001800.4:c.141+127C>A MANE Select NP_001791.1:n.141+127C>A
NM_079421.3:c.141+127C>A NP_524145.1:n.141+127C>A