Canonical Allele Identifier: CA2619241275

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55971929G>T , CM000674.2:g.55971929G>T GRCh38
NC_000012.11:g.56365713G>T , CM000674.1:g.56365713G>T GRCh37
NC_000012.10:g.54651980G>T NCBI36
NG_034014.1:g.10161G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266970.9:c.*304G>T (CDK2) MANE Select ENSP00000266970.4:n.*304G>T
ENST00000266970.8:c.*304G>T (CDK2) ENSP00000266970.4:n.*304G>T
ENST00000549233.2:c.-95-162C>A (PMEL) ENSP00000448871.1:n.-95-162C>A
ENST00000553376.5:c.*304G>T (CDK2) ENSP00000452514.1:n.*304G>T
ENST00000555408.5:c.*1813G>T (CDK2) ENSP00000450983.1:n.*1813G>T
NM_001290230.1:c.*304G>T (CDK2) NP_001277159.1:n.*304G>T
NM_001798.4:c.*304G>T (CDK2) NP_001789.2:n.*304G>T
NM_052827.3:c.*304G>T (CDK2) NP_439892.2:n.*304G>T
XM_011537732.1:c.*304G>T (CDK2) XP_011536034.1:n.*304G>T
XM_011537732.2:c.*304G>T (CDK2) XP_011536034.1:n.*304G>T
NM_001798.5:c.*304G>T (CDK2) MANE Select NP_001789.2:n.*304G>T
NM_001290230.2:c.*304G>T (CDK2) NP_001277159.1:n.*304G>T
NM_052827.4:c.*304G>T (CDK2) NP_439892.2:n.*304G>T