Canonical Allele Identifier: CA2038170909

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55971939A= , CM000674.2:g.55971939A= GRCh38
NC_000012.11:g.56365723A= , CM000674.1:g.56365723A= GRCh37
NC_000012.10:g.54651990A= NCBI36
NG_034014.1:g.10171A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266970.9:c.*314A= (CDK2) MANE Select ENSP00000266970.4:n.*314A=
ENST00000266970.8:c.*314A= (CDK2) ENSP00000266970.4:n.*314A=
ENST00000549233.2:c.-95-172T= (PMEL) ENSP00000448871.1:n.-95-172T=
ENST00000553376.5:c.*314A= (CDK2) ENSP00000452514.1:n.*314A=
ENST00000555408.5:c.*1823A= (CDK2) ENSP00000450983.1:n.*1823A=
NM_001290230.1:c.*314A= (CDK2) NP_001277159.1:n.*314A=
NM_001798.4:c.*314A= (CDK2) NP_001789.2:n.*314A=
NM_052827.3:c.*314A= (CDK2) NP_439892.2:n.*314A=
XM_011537732.1:c.*314A= (CDK2) XP_011536034.1:n.*314A=
XM_011537732.2:c.*314A= (CDK2) XP_011536034.1:n.*314A=
NM_001798.5:c.*314A= (CDK2) MANE Select NP_001789.2:n.*314A=
NM_001290230.2:c.*314A= (CDK2) NP_001277159.1:n.*314A=
NM_052827.4:c.*314A= (CDK2) NP_439892.2:n.*314A=