Canonical Allele Identifier: CA2038994126

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750188T= , CM000674.2:g.57750188T=	GRCh38
NC_000012.11:g.58143971T= , CM000674.1:g.58143971T=	GRCh37
NC_000012.10:g.56430238T=	NCBI36
NG_007484.2:g.7194A= , LRG_490:g.7194A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+468A= (CDK4) MANE Select	ENSP00000257904.5:n.632+468A=
ENST00000257910.8:c.*2898T= (TSPAN31) MANE Select	ENSP00000257910.3:n.*2898T=
ENST00000257904.10:c.632+468A= (CDK4)	ENSP00000257904.5:n.632+468A=
ENST00000312990.10:c.280+468A= (CDK4)	ENSP00000316889.6:n.280+468A=
ENST00000546489.5:c.410+468A= (CDK4)	ENSP00000447779.1:n.410+468A=
ENST00000547281.5:c.410+468A= (CDK4)	ENSP00000447274.1:n.410+468A=
ENST00000547992.5:c.*2898T= (TSPAN31)	ENSP00000448209.1:n.*2898T=
ENST00000549606.5:c.-157-684A= (CDK4)	ENSP00000447005.1:n.-157-684A=
ENST00000550419.5:c.*38+254A= (CDK4)	ENSP00000448098.1:n.*38+254A=
ENST00000551888.5:n.458+468A= (CDK4)
ENST00000553237.5:c.*271+468A= (CDK4)	ENSP00000448885.1:n.*271+468A=
NM_000075.3:c.632+468A= (CDK4)	NP_000066.1:n.632+468A=
NM_000075.4:c.632+468A= (CDK4) MANE Select	NP_000066.1:n.632+468A=
NM_005981.5:c.*2898T= (TSPAN31) MANE Select	NP_005972.1:n.*2898T=
NM_001330168.2:c.*2898T= (TSPAN31)	NP_001317097.1:n.*2898T=
NM_001330169.2:c.*2898T= (TSPAN31)	NP_001317098.1:n.*2898T=