Canonical Allele Identifier: CA404021578

Gene: CDKN2D

Linked Data

• gnomAD v4: 19-10568574-A-G
• MyVariant Identifiers: chr19:g.10679250A>G (hg19) ; chr19:g.10568574A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10568574A>G , CM000681.2:g.10568574A>G	GRCh38
NC_000019.9:g.10679250A>G , CM000681.1:g.10679250A>G	GRCh37
NC_000019.8:g.10540250A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393599.3:c.80T>C MANE Select	ENSP00000377224.1:p.Leu27Pro
ENST00000335766.2:c.80T>C	ENSP00000337056.1:p.Leu27Pro
ENST00000393599.2:c.80T>C	ENSP00000377224.1:p.Leu27Pro
NM_001800.3:c.80T>C	NP_001791.1:p.Leu27Pro
NM_079421.2:c.80T>C	NP_524145.1:p.Leu27Pro
NM_001800.4:c.80T>C MANE Select	NP_001791.1:p.Leu27Pro
NM_079421.3:c.80T>C	NP_524145.1:p.Leu27Pro