Canonical Allele Identifier: CA2322494173
Gene: CDKN2D HGNC NCBI

Linked Data

dbSNP Id: rs1916959632
gnomAD v4: 19-10568390-AGAG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568391_10568393del , CM000681.2:g.10568391_10568393del GRCh38
NC_000019.9:g.10679067_10679069del , CM000681.1:g.10679067_10679069del GRCh37
NC_000019.8:g.10540067_10540069del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.141+120_141+122del MANE Select ENSP00000377224.1:n.141+120_141+122del
ENST00000335766.2:c.141+120_141+122del ENSP00000337056.1:n.141+120_141+122del
ENST00000393599.2:c.141+120_141+122del ENSP00000377224.1:n.141+120_141+122del
NM_001800.3:c.141+120_141+122del NP_001791.1:n.141+120_141+122del
NM_079421.2:c.141+120_141+122del NP_524145.1:n.141+120_141+122del
NM_001800.4:c.141+120_141+122del MANE Select NP_001791.1:n.141+120_141+122del
NM_079421.3:c.141+120_141+122del NP_524145.1:n.141+120_141+122del
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