Canonical Allele Identifier: CA919097379

Gene: CDK4 TSPAN31

Linked Data

• dbSNP Id: rs1555201194

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750192_57750201del , CM000674.2:g.57750192_57750201del	GRCh38
NC_000012.11:g.58143975_58143984del , CM000674.1:g.58143975_58143984del	GRCh37
NC_000012.10:g.56430242_56430251del	NCBI36
NG_007484.2:g.7184_7193del , LRG_490:g.7184_7193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+458_632+467del (CDK4) MANE Select	ENSP00000257904.5:n.632+458_632+467del
ENST00000257910.8:c.*2902_*2911del (TSPAN31) MANE Select	ENSP00000257910.3:n.*2902_*2911del
ENST00000257904.10:c.632+458_632+467del (CDK4)	ENSP00000257904.5:n.632+458_632+467del
ENST00000312990.10:c.280+458_280+467del (CDK4)	ENSP00000316889.6:n.280+458_280+467del
ENST00000546489.5:c.410+458_410+467del (CDK4)	ENSP00000447779.1:n.410+458_410+467del
ENST00000547281.5:c.410+458_410+467del (CDK4)	ENSP00000447274.1:n.410+458_410+467del
ENST00000547992.5:c.*2902_*2911del (TSPAN31)	ENSP00000448209.1:n.*2902_*2911del
ENST00000549606.5:c.-157-694_-157-685del (CDK4)	ENSP00000447005.1:n.-157-694_-157-685del
ENST00000550419.5:c.*38+244_*38+253del (CDK4)	ENSP00000448098.1:n.*38+244_*38+253del
ENST00000551888.5:n.458+458_458+467del (CDK4)
ENST00000553237.5:c.*271+458_*271+467del (CDK4)	ENSP00000448885.1:n.*271+458_*271+467del
NM_000075.3:c.632+458_632+467del (CDK4)	NP_000066.1:n.632+458_632+467del
NM_000075.4:c.632+458_632+467del (CDK4) MANE Select	NP_000066.1:n.632+458_632+467del
NM_005981.5:c.*2902_*2911del (TSPAN31) MANE Select	NP_005972.1:n.*2902_*2911del
NM_001330168.2:c.*2902_*2911del (TSPAN31)	NP_001317097.1:n.*2902_*2911del
NM_001330169.2:c.*2902_*2911del (TSPAN31)	NP_001317098.1:n.*2902_*2911del