Canonical Allele Identifier: CA2582401921
Gene: CDKN2D HGNC NCBI

Linked Data

gnomAD v4: 19-10568388-CTA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568389_10568390del , CM000681.2:g.10568389_10568390del GRCh38
NC_000019.9:g.10679065_10679066del , CM000681.1:g.10679065_10679066del GRCh37
NC_000019.8:g.10540065_10540066del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393599.3:c.141+123_141+124del MANE Select ENSP00000377224.1:n.141+123_141+124del
ENST00000335766.2:c.141+123_141+124del ENSP00000337056.1:n.141+123_141+124del
ENST00000393599.2:c.141+123_141+124del ENSP00000377224.1:n.141+123_141+124del
NM_001800.3:c.141+123_141+124del NP_001791.1:n.141+123_141+124del
NM_079421.2:c.141+123_141+124del NP_524145.1:n.141+123_141+124del
NM_001800.4:c.141+123_141+124del MANE Select NP_001791.1:n.141+123_141+124del
NM_079421.3:c.141+123_141+124del NP_524145.1:n.141+123_141+124del
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