Canonical Allele Identifier: CA2038168986

Gene: CDK2 PMEL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55970537A= , CM000674.2:g.55970537A=	GRCh38
NC_000012.11:g.56364321A= , CM000674.1:g.56364321A=	GRCh37
NC_000012.10:g.54650588A=	NCBI36
NG_028086.1:g.1176T=
NG_034014.1:g.8769A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001798.5:c.589-507A= (CDK2) MANE Select	NP_001789.2:n.589-507A=
ENST00000266970.9:c.589-507A= (CDK2) MANE Select	ENSP00000266970.4:n.589-507A=
NM_001290230.1:c.409-507A= (CDK2)	NP_001277159.1:n.409-507A=
NM_001290230.2:c.409-507A= (CDK2)	NP_001277159.1:n.409-507A=
NM_001798.4:c.589-507A= (CDK2)	NP_001789.2:n.589-507A=
NM_052827.3:c.487-507A= (CDK2)	NP_439892.2:n.487-507A=
NM_052827.4:c.487-507A= (CDK2)	NP_439892.2:n.487-507A=
ENST00000266970.8:c.589-507A= (CDK2)	ENSP00000266970.4:n.589-507A=
ENST00000354056.4:c.487-507A= (CDK2)	ENSP00000243067.4:n.487-507A=
ENST00000440311.6:c.409-507A= (CDK2)	ENSP00000393605.2:n.409-507A=
ENST00000549233.2:c.85+416T= (PMEL)	ENSP00000448871.1:n.85+416T=
ENST00000553376.5:c.589-61A= (CDK2)	ENSP00000452514.1:n.589-61A=
ENST00000555408.5:c.*1201-507A= (CDK2)	ENSP00000450983.1:n.*1201-507A=
ENST00000556146.1:n.868-507A= (CDK2)
ENST00000556276.5:n.610-507A= (CDK2)
ENST00000556464.5:n.554-507A= (CDK2)
ENST00000556656.5:n.555-507A= (CDK2)
XM_011537732.1:c.589-61A= (CDK2)	XP_011536034.1:n.589-61A=
XM_011537732.2:c.589-61A= (CDK2)	XP_011536034.1:n.589-61A=