Canonical Allele Identifier: CA2499221772
Gene: CDK4 HGNC NCBI
TSPAN31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57749446del , CM000674.2:g.57749446del GRCh38
NC_000012.11:g.58143229del , CM000674.1:g.58143229del GRCh37
NC_000012.10:g.56429496del NCBI36
NG_007484.2:g.7936del , LRG_490:g.7936del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.683+8del (CDK4) MANE Select ENSP00000257904.5:n.683+8del
ENST00000257910.8:c.*2156del (TSPAN31) MANE Select ENSP00000257910.3:n.*2156del
ENST00000257904.10:c.683+8del (CDK4) ENSP00000257904.5:n.683+8del
ENST00000312990.10:c.331+8del (CDK4) ENSP00000316889.6:n.331+8del
ENST00000546489.5:c.461+8del (CDK4) ENSP00000447779.1:n.461+8del
ENST00000547281.5:c.461+8del (CDK4) ENSP00000447274.1:n.461+8del
ENST00000547992.5:c.*2156del (TSPAN31) ENSP00000448209.1:n.*2156del
ENST00000549606.5:c.-107+8del (CDK4) ENSP00000447005.1:n.-107+8del
ENST00000550419.5:c.*89+8del (CDK4) ENSP00000448098.1:n.*89+8del
ENST00000551888.5:n.509+8del (CDK4)
ENST00000552713.5:n.342+8del (CDK4)
ENST00000553237.5:c.*322+8del (CDK4) ENSP00000448885.1:n.*322+8del
NM_000075.3:c.683+8del (CDK4) NP_000066.1:n.683+8del
NM_000075.4:c.683+8del (CDK4) MANE Select NP_000066.1:n.683+8del
NM_005981.5:c.*2156del (TSPAN31) MANE Select NP_005972.1:n.*2156del
NM_001330168.2:c.*2156del (TSPAN31) NP_001317097.1:n.*2156del
NM_001330169.2:c.*2156del (TSPAN31) NP_001317098.1:n.*2156del