Canonical Allele Identifier: CA2038170915

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55971945C= , CM000674.2:g.55971945C= GRCh38
NC_000012.11:g.56365729C= , CM000674.1:g.56365729C= GRCh37
NC_000012.10:g.54651996C= NCBI36
NG_034014.1:g.10177C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266970.9:c.*320C= (CDK2) MANE Select ENSP00000266970.4:n.*320C=
ENST00000266970.8:c.*320C= (CDK2) ENSP00000266970.4:n.*320C=
ENST00000549233.2:c.-95-178G= (PMEL) ENSP00000448871.1:n.-95-178G=
ENST00000553376.5:c.*320C= (CDK2) ENSP00000452514.1:n.*320C=
ENST00000555408.5:c.*1829C= (CDK2) ENSP00000450983.1:n.*1829C=
NM_001290230.1:c.*320C= (CDK2) NP_001277159.1:n.*320C=
NM_001798.4:c.*320C= (CDK2) NP_001789.2:n.*320C=
NM_052827.3:c.*320C= (CDK2) NP_439892.2:n.*320C=
XM_011537732.1:c.*320C= (CDK2) XP_011536034.1:n.*320C=
XM_011537732.2:c.*320C= (CDK2) XP_011536034.1:n.*320C=
NM_001798.5:c.*320C= (CDK2) MANE Select NP_001789.2:n.*320C=
NM_001290230.2:c.*320C= (CDK2) NP_001277159.1:n.*320C=
NM_052827.4:c.*320C= (CDK2) NP_439892.2:n.*320C=