Canonical Allele Identifier: CA6657623

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57748574C>T , CM000674.2:g.57748574C>T	GRCh38
NC_000012.11:g.58142357C>T , CM000674.1:g.58142357C>T	GRCh37
NC_000012.10:g.56428624C>T	NCBI36
NG_007484.2:g.8808G>A , LRG_490:g.8808G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.863G>A (CDK4) MANE Select	ENSP00000257904.5:p.Arg288Gln
ENST00000257910.8:c.*1284C>T (TSPAN31) MANE Select	ENSP00000257910.3:n.*1284C>T
ENST00000257904.10:c.863G>A (CDK4)	ENSP00000257904.5:p.Arg288Gln
ENST00000312990.10:c.*175G>A (CDK4)	ENSP00000316889.6:n.*175G>A
ENST00000547992.5:c.*1284C>T (TSPAN31)	ENSP00000448209.1:n.*1284C>T
ENST00000549606.5:c.74G>A (CDK4)	ENSP00000447005.1:p.Arg25Gln
ENST00000552713.5:n.522G>A (CDK4)
ENST00000553237.5:c.*502G>A (CDK4)	ENSP00000448885.1:n.*502G>A
NM_000075.3:c.863G>A (CDK4)	NP_000066.1:p.Arg288Gln
NM_000075.4:c.863G>A (CDK4) MANE Select	NP_000066.1:p.Arg288Gln
NM_005981.5:c.*1284C>T (TSPAN31) MANE Select	NP_005972.1:n.*1284C>T
NM_001330168.2:c.*1284C>T (TSPAN31)	NP_001317097.1:n.*1284C>T
NM_001330169.2:c.*1284C>T (TSPAN31)	NP_001317098.1:n.*1284C>T