Canonical Allele Identifier: CA2038994096

Gene: CDK4 TSPAN31

Linked Data

• dbSNP Id: rs1848889125

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750184_57750192del , CM000674.2:g.57750184_57750192del	GRCh38
NC_000012.11:g.58143967_58143975del , CM000674.1:g.58143967_58143975del	GRCh37
NC_000012.10:g.56430234_56430242del	NCBI36
NG_007484.2:g.7190_7198del , LRG_490:g.7190_7198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+464_632+472del (CDK4) MANE Select	ENSP00000257904.5:n.632+464_632+472del
ENST00000257910.8:c.*2894_*2902del (TSPAN31) MANE Select	ENSP00000257910.3:n.*2894_*2902del
ENST00000257904.10:c.632+464_632+472del (CDK4)	ENSP00000257904.5:n.632+464_632+472del
ENST00000312990.10:c.280+464_280+472del (CDK4)	ENSP00000316889.6:n.280+464_280+472del
ENST00000546489.5:c.410+464_410+472del (CDK4)	ENSP00000447779.1:n.410+464_410+472del
ENST00000547281.5:c.410+464_410+472del (CDK4)	ENSP00000447274.1:n.410+464_410+472del
ENST00000547992.5:c.*2894_*2902del (TSPAN31)	ENSP00000448209.1:n.*2894_*2902del
ENST00000549606.5:c.-157-688_-157-680del (CDK4)	ENSP00000447005.1:n.-157-688_-157-680del
ENST00000550419.5:c.*38+250_*38+258del (CDK4)	ENSP00000448098.1:n.*38+250_*38+258del
ENST00000551888.5:n.458+464_458+472del (CDK4)
ENST00000553237.5:c.*271+464_*271+472del (CDK4)	ENSP00000448885.1:n.*271+464_*271+472del
NM_000075.3:c.632+464_632+472del (CDK4)	NP_000066.1:n.632+464_632+472del
NM_000075.4:c.632+464_632+472del (CDK4) MANE Select	NP_000066.1:n.632+464_632+472del
NM_005981.5:c.*2894_*2902del (TSPAN31) MANE Select	NP_005972.1:n.*2894_*2902del
NM_001330168.2:c.*2894_*2902del (TSPAN31)	NP_001317097.1:n.*2894_*2902del
NM_001330169.2:c.*2894_*2902del (TSPAN31)	NP_001317098.1:n.*2894_*2902del