Canonical Allele Identifier: CA2038171336

Gene: CDK2 PMEL

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55972376G>A , CM000674.2:g.55972376G>A	GRCh38
NC_000012.11:g.56366160G>A , CM000674.1:g.56366160G>A	GRCh37
NC_000012.10:g.54652427G>A	NCBI36
NG_034014.1:g.10608G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266970.9:c.*751G>A (CDK2) MANE Select	ENSP00000266970.4:n.*751G>A
ENST00000266970.8:c.*751G>A (CDK2)	ENSP00000266970.4:n.*751G>A
ENST00000549233.2:c.-95-609C>T (PMEL)	ENSP00000448871.1:n.-95-609C>T
ENST00000555408.5:c.*2260G>A (CDK2)	ENSP00000450983.1:n.*2260G>A
NM_001290230.1:c.*751G>A (CDK2)	NP_001277159.1:n.*751G>A
NM_001798.4:c.*751G>A (CDK2)	NP_001789.2:n.*751G>A
NM_052827.3:c.*751G>A (CDK2)	NP_439892.2:n.*751G>A
XM_011537732.1:c.*751G>A (CDK2)	XP_011536034.1:n.*751G>A
XM_011537732.2:c.*751G>A (CDK2)	XP_011536034.1:n.*751G>A
NM_001798.5:c.*751G>A (CDK2) MANE Select	NP_001789.2:n.*751G>A
NM_001290230.2:c.*751G>A (CDK2)	NP_001277159.1:n.*751G>A
NM_052827.4:c.*751G>A (CDK2)	NP_439892.2:n.*751G>A