Canonical Allele Identifier: CA385542665
Gene: CDK4 HGNC NCBI
TSPAN31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57748616T>C , CM000674.2:g.57748616T>C GRCh38
NC_000012.11:g.58142399T>C , CM000674.1:g.58142399T>C GRCh37
NC_000012.10:g.56428666T>C NCBI36
NG_007484.2:g.8766A>G , LRG_490:g.8766A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.821A>G (CDK4) MANE Select ENSP00000257904.5:p.Glu274Gly
ENST00000257910.8:c.*1326T>C (TSPAN31) MANE Select ENSP00000257910.3:n.*1326T>C
ENST00000257904.10:c.821A>G (CDK4) ENSP00000257904.5:p.Glu274Gly
ENST00000312990.10:c.*133A>G (CDK4) ENSP00000316889.6:n.*133A>G
ENST00000546489.5:c.599A>G (CDK4) ENSP00000447779.1:p.Glu200Gly
ENST00000547992.5:c.*1326T>C (TSPAN31) ENSP00000448209.1:n.*1326T>C
ENST00000549606.5:c.32A>G (CDK4) ENSP00000447005.1:p.Glu11Gly
ENST00000552713.5:n.480A>G (CDK4)
ENST00000553237.5:c.*460A>G (CDK4) ENSP00000448885.1:n.*460A>G
NM_000075.3:c.821A>G (CDK4) NP_000066.1:p.Glu274Gly
NM_000075.4:c.821A>G (CDK4) MANE Select NP_000066.1:p.Glu274Gly
NM_005981.5:c.*1326T>C (TSPAN31) MANE Select NP_005972.1:n.*1326T>C
NM_001330168.2:c.*1326T>C (TSPAN31) NP_001317097.1:n.*1326T>C
NM_001330169.2:c.*1326T>C (TSPAN31) NP_001317098.1:n.*1326T>C