Canonical Allele Identifier: CA2038994143

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750189_57750192delinsAAAT , CM000674.2:g.57750189_57750192delinsAAAT	GRCh38
NC_000012.11:g.58143972_58143975delinsAAAT , CM000674.1:g.58143972_58143975delinsAAAT	GRCh37
NC_000012.10:g.56430239_56430242delinsAAAT	NCBI36
NG_007484.2:g.7190_7193delinsATTT , LRG_490:g.7190_7193delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+464_632+467delinsATTT (CDK4) MANE Select	ENSP00000257904.5:n.632+464_632+467delinsATTT
ENST00000257910.8:c.*2899_*2902delinsAAAT (TSPAN31) MANE Select	ENSP00000257910.3:n.*2899_*2902delinsAAAT
ENST00000257904.10:c.632+464_632+467delinsATTT (CDK4)	ENSP00000257904.5:n.632+464_632+467delinsATTT
ENST00000312990.10:c.280+464_280+467delinsATTT (CDK4)	ENSP00000316889.6:n.280+464_280+467delinsATTT
ENST00000546489.5:c.410+464_410+467delinsATTT (CDK4)	ENSP00000447779.1:n.410+464_410+467delinsATTT
ENST00000547281.5:c.410+464_410+467delinsATTT (CDK4)	ENSP00000447274.1:n.410+464_410+467delinsATTT
ENST00000547992.5:c.*2899_*2902delinsAAAT (TSPAN31)	ENSP00000448209.1:n.*2899_*2902delinsAAAT
ENST00000549606.5:c.-157-688_-157-685delinsATTT (CDK4)	ENSP00000447005.1:n.-157-688_-157-685delinsATTT
ENST00000550419.5:c.*38+250_*38+253delinsATTT (CDK4)	ENSP00000448098.1:n.*38+250_*38+253delinsATTT
ENST00000551888.5:n.458+464_458+467delinsATTT (CDK4)
ENST00000553237.5:c.*271+464_*271+467delinsATTT (CDK4)	ENSP00000448885.1:n.*271+464_*271+467delinsATTT
NM_000075.3:c.632+464_632+467delinsATTT (CDK4)	NP_000066.1:n.632+464_632+467delinsATTT
NM_000075.4:c.632+464_632+467delinsATTT (CDK4) MANE Select	NP_000066.1:n.632+464_632+467delinsATTT
NM_005981.5:c.*2899_*2902delinsAAAT (TSPAN31) MANE Select	NP_005972.1:n.*2899_*2902delinsAAAT
NM_001330168.2:c.*2899_*2902delinsAAAT (TSPAN31)	NP_001317097.1:n.*2899_*2902delinsAAAT
NM_001330169.2:c.*2899_*2902delinsAAAT (TSPAN31)	NP_001317098.1:n.*2899_*2902delinsAAAT