Canonical Allele Identifier: CA385543157

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57749219A>G , CM000674.2:g.57749219A>G	GRCh38
NC_000012.11:g.58143002A>G , CM000674.1:g.58143002A>G	GRCh37
NC_000012.10:g.56429269A>G	NCBI36
NG_007484.2:g.8163T>C , LRG_490:g.8163T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.782T>C (CDK4) MANE Select	ENSP00000257904.5:p.Val261Ala
ENST00000257910.8:c.*1929A>G (TSPAN31) MANE Select	ENSP00000257910.3:n.*1929A>G
ENST00000257904.10:c.782T>C (CDK4)	ENSP00000257904.5:p.Val261Ala
ENST00000312990.10:c.*94T>C (CDK4)	ENSP00000316889.6:n.*94T>C
ENST00000546489.5:c.560T>C (CDK4)	ENSP00000447779.1:p.Val187Ala
ENST00000547992.5:c.*1929A>G (TSPAN31)	ENSP00000448209.1:n.*1929A>G
ENST00000549606.5:c.-8T>C (CDK4)	ENSP00000447005.1:n.-8T>C
ENST00000551888.5:n.608T>C (CDK4)
ENST00000552713.5:n.441T>C (CDK4)
ENST00000553237.5:c.*421T>C (CDK4)	ENSP00000448885.1:n.*421T>C
NM_000075.3:c.782T>C (CDK4)	NP_000066.1:p.Val261Ala
NM_000075.4:c.782T>C (CDK4) MANE Select	NP_000066.1:p.Val261Ala
NM_005981.5:c.*1929A>G (TSPAN31) MANE Select	NP_005972.1:n.*1929A>G
NM_001330168.2:c.*1929A>G (TSPAN31)	NP_001317097.1:n.*1929A>G
NM_001330169.2:c.*1929A>G (TSPAN31)	NP_001317098.1:n.*1929A>G