Canonical Allele Identifier: CA385543332

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57749249G>A , CM000674.2:g.57749249G>A	GRCh38
NC_000012.11:g.58143032G>A , CM000674.1:g.58143032G>A	GRCh37
NC_000012.10:g.56429299G>A	NCBI36
NG_007484.2:g.8133C>T , LRG_490:g.8133C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.752C>T (CDK4) MANE Select	ENSP00000257904.5:p.Pro251Leu
ENST00000257910.8:c.*1959G>A (TSPAN31) MANE Select	ENSP00000257910.3:n.*1959G>A
ENST00000257904.10:c.752C>T (CDK4)	ENSP00000257904.5:p.Pro251Leu
ENST00000312990.10:c.*64C>T (CDK4)	ENSP00000316889.6:n.*64C>T
ENST00000546489.5:c.530C>T (CDK4)	ENSP00000447779.1:p.Pro177Leu
ENST00000547281.5:c.530C>T (CDK4)	ENSP00000447274.1:p.Pro177Leu
ENST00000547992.5:c.*1959G>A (TSPAN31)	ENSP00000448209.1:n.*1959G>A
ENST00000549606.5:c.-38C>T (CDK4)	ENSP00000447005.1:n.-38C>T
ENST00000550419.5:c.*158C>T (CDK4)	ENSP00000448098.1:n.*158C>T
ENST00000551888.5:n.578C>T (CDK4)
ENST00000552713.5:n.411C>T (CDK4)
ENST00000553237.5:c.*391C>T (CDK4)	ENSP00000448885.1:n.*391C>T
NM_000075.3:c.752C>T (CDK4)	NP_000066.1:p.Pro251Leu
NM_000075.4:c.752C>T (CDK4) MANE Select	NP_000066.1:p.Pro251Leu
NM_005981.5:c.*1959G>A (TSPAN31) MANE Select	NP_005972.1:n.*1959G>A
NM_001330168.2:c.*1959G>A (TSPAN31)	NP_001317097.1:n.*1959G>A
NM_001330169.2:c.*1959G>A (TSPAN31)	NP_001317098.1:n.*1959G>A