Canonical Allele Identifier: CA2619241277

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55971935C>T , CM000674.2:g.55971935C>T GRCh38
NC_000012.11:g.56365719C>T , CM000674.1:g.56365719C>T GRCh37
NC_000012.10:g.54651986C>T NCBI36
NG_034014.1:g.10167C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266970.9:c.*310C>T (CDK2) MANE Select ENSP00000266970.4:n.*310C>T
ENST00000266970.8:c.*310C>T (CDK2) ENSP00000266970.4:n.*310C>T
ENST00000549233.2:c.-95-168G>A (PMEL) ENSP00000448871.1:n.-95-168G>A
ENST00000553376.5:c.*310C>T (CDK2) ENSP00000452514.1:n.*310C>T
ENST00000555408.5:c.*1819C>T (CDK2) ENSP00000450983.1:n.*1819C>T
NM_001290230.1:c.*310C>T (CDK2) NP_001277159.1:n.*310C>T
NM_001798.4:c.*310C>T (CDK2) NP_001789.2:n.*310C>T
NM_052827.3:c.*310C>T (CDK2) NP_439892.2:n.*310C>T
XM_011537732.1:c.*310C>T (CDK2) XP_011536034.1:n.*310C>T
XM_011537732.2:c.*310C>T (CDK2) XP_011536034.1:n.*310C>T
NM_001798.5:c.*310C>T (CDK2) MANE Select NP_001789.2:n.*310C>T
NM_001290230.2:c.*310C>T (CDK2) NP_001277159.1:n.*310C>T
NM_052827.4:c.*310C>T (CDK2) NP_439892.2:n.*310C>T