Canonical Allele Identifier: CA385542309

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57748556T>C , CM000674.2:g.57748556T>C	GRCh38
NC_000012.11:g.58142339T>C , CM000674.1:g.58142339T>C	GRCh37
NC_000012.10:g.56428606T>C	NCBI36
NG_007484.2:g.8826A>G , LRG_490:g.8826A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.881A>G (CDK4) MANE Select	ENSP00000257904.5:p.Tyr294Cys
ENST00000257910.8:c.*1266T>C (TSPAN31) MANE Select	ENSP00000257910.3:n.*1266T>C
ENST00000257904.10:c.881A>G (CDK4)	ENSP00000257904.5:p.Tyr294Cys
ENST00000312990.10:c.*193A>G (CDK4)	ENSP00000316889.6:n.*193A>G
ENST00000547992.5:c.*1266T>C (TSPAN31)	ENSP00000448209.1:n.*1266T>C
ENST00000549606.5:c.92A>G (CDK4)	ENSP00000447005.1:p.Tyr31Cys
ENST00000552713.5:n.540A>G (CDK4)
ENST00000553237.5:c.*520A>G (CDK4)	ENSP00000448885.1:n.*520A>G
NM_000075.3:c.881A>G (CDK4)	NP_000066.1:p.Tyr294Cys
NM_000075.4:c.881A>G (CDK4) MANE Select	NP_000066.1:p.Tyr294Cys
NM_005981.5:c.*1266T>C (TSPAN31) MANE Select	NP_005972.1:n.*1266T>C
NM_001330168.2:c.*1266T>C (TSPAN31)	NP_001317097.1:n.*1266T>C
NM_001330169.2:c.*1266T>C (TSPAN31)	NP_001317098.1:n.*1266T>C