Canonical Allele Identifier: CA15730372

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57749071C>A , CM000674.2:g.57749071C>A	GRCh38
NC_000012.11:g.58142854C>A , CM000674.1:g.58142854C>A	GRCh37
NC_000012.10:g.56429121C>A	NCBI36
NG_007484.2:g.8311G>T , LRG_490:g.8311G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.819+111G>T (CDK4) MANE Select	ENSP00000257904.5:n.819+111G>T
ENST00000257910.8:c.*1781C>A (TSPAN31) MANE Select	ENSP00000257910.3:n.*1781C>A
ENST00000257904.10:c.819+111G>T (CDK4)	ENSP00000257904.5:n.819+111G>T
ENST00000312990.10:c.*131+111G>T (CDK4)	ENSP00000316889.6:n.*131+111G>T
ENST00000546489.5:c.597+111G>T (CDK4)	ENSP00000447779.1:n.597+111G>T
ENST00000547992.5:c.*1781C>A (TSPAN31)	ENSP00000448209.1:n.*1781C>A
ENST00000549606.5:c.30+111G>T (CDK4)	ENSP00000447005.1:n.30+111G>T
ENST00000552713.5:n.478+111G>T (CDK4)
ENST00000553237.5:c.*458+111G>T (CDK4)	ENSP00000448885.1:n.*458+111G>T
NM_000075.3:c.819+111G>T (CDK4)	NP_000066.1:n.819+111G>T
NM_000075.4:c.819+111G>T (CDK4) MANE Select	NP_000066.1:n.819+111G>T
NM_005981.5:c.*1781C>A (TSPAN31) MANE Select	NP_005972.1:n.*1781C>A
NM_001330168.2:c.*1781C>A (TSPAN31)	NP_001317097.1:n.*1781C>A
NM_001330169.2:c.*1781C>A (TSPAN31)	NP_001317098.1:n.*1781C>A