Canonical Allele Identifier: CA2038993988

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750153_57750156delinsCAAT , CM000674.2:g.57750153_57750156delinsCAAT	GRCh38
NC_000012.11:g.58143936_58143939delinsCAAT , CM000674.1:g.58143936_58143939delinsCAAT	GRCh37
NC_000012.10:g.56430203_56430206delinsCAAT	NCBI36
NG_007484.2:g.7226_7229delinsATTG , LRG_490:g.7226_7229delinsATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+500_632+503delinsATTG (CDK4) MANE Select	ENSP00000257904.5:n.632+500_632+503delinsATTG
ENST00000257910.8:c.*2863_*2866delinsCAAT (TSPAN31) MANE Select	ENSP00000257910.3:n.*2863_*2866delinsCAAT
ENST00000257904.10:c.632+500_632+503delinsATTG (CDK4)	ENSP00000257904.5:n.632+500_632+503delinsATTG
ENST00000312990.10:c.280+500_280+503delinsATTG (CDK4)	ENSP00000316889.6:n.280+500_280+503delinsATTG
ENST00000546489.5:c.410+500_410+503delinsATTG (CDK4)	ENSP00000447779.1:n.410+500_410+503delinsATTG
ENST00000547281.5:c.410+500_410+503delinsATTG (CDK4)	ENSP00000447274.1:n.410+500_410+503delinsATTG
ENST00000547992.5:c.*2863_*2866delinsCAAT (TSPAN31)	ENSP00000448209.1:n.*2863_*2866delinsCAAT
ENST00000549606.5:c.-157-652_-157-649delinsATTG (CDK4)	ENSP00000447005.1:n.-157-652_-157-649delinsATTG
ENST00000550419.5:c.*38+286_*38+289delinsATTG (CDK4)	ENSP00000448098.1:n.*38+286_*38+289delinsATTG
ENST00000551888.5:n.458+500_458+503delinsATTG (CDK4)
ENST00000553237.5:c.*271+500_*271+503delinsATTG (CDK4)	ENSP00000448885.1:n.*271+500_*271+503delinsATTG
NM_000075.3:c.632+500_632+503delinsATTG (CDK4)	NP_000066.1:n.632+500_632+503delinsATTG
NM_000075.4:c.632+500_632+503delinsATTG (CDK4) MANE Select	NP_000066.1:n.632+500_632+503delinsATTG
NM_005981.5:c.*2863_*2866delinsCAAT (TSPAN31) MANE Select	NP_005972.1:n.*2863_*2866delinsCAAT
NM_001330168.2:c.*2863_*2866delinsCAAT (TSPAN31)	NP_001317097.1:n.*2863_*2866delinsCAAT
NM_001330169.2:c.*2863_*2866delinsCAAT (TSPAN31)	NP_001317098.1:n.*2863_*2866delinsCAAT