Canonical Allele Identifier: CA2619241262

Gene: CDK2 PMEL

Linked Data

• gnomAD v4: 12-55971924-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55971924C>G , CM000674.2:g.55971924C>G	GRCh38
NC_000012.11:g.56365708C>G , CM000674.1:g.56365708C>G	GRCh37
NC_000012.10:g.54651975C>G	NCBI36
NG_034014.1:g.10156C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266970.9:c.*299C>G (CDK2) MANE Select	ENSP00000266970.4:n.*299C>G
ENST00000266970.8:c.*299C>G (CDK2)	ENSP00000266970.4:n.*299C>G
ENST00000549233.2:c.-95-157G>C (PMEL)	ENSP00000448871.1:n.-95-157G>C
ENST00000553376.5:c.*299C>G (CDK2)	ENSP00000452514.1:n.*299C>G
ENST00000555408.5:c.*1808C>G (CDK2)	ENSP00000450983.1:n.*1808C>G
NM_001290230.1:c.*299C>G (CDK2)	NP_001277159.1:n.*299C>G
NM_001798.4:c.*299C>G (CDK2)	NP_001789.2:n.*299C>G
NM_052827.3:c.*299C>G (CDK2)	NP_439892.2:n.*299C>G
XM_011537732.1:c.*299C>G (CDK2)	XP_011536034.1:n.*299C>G
XM_011537732.2:c.*299C>G (CDK2)	XP_011536034.1:n.*299C>G
NM_001798.5:c.*299C>G (CDK2) MANE Select	NP_001789.2:n.*299C>G
NM_001290230.2:c.*299C>G (CDK2)	NP_001277159.1:n.*299C>G
NM_052827.4:c.*299C>G (CDK2)	NP_439892.2:n.*299C>G