Canonical Allele Identifier: CA2038994064

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750177_57750180delinsAAAT , CM000674.2:g.57750177_57750180delinsAAAT	GRCh38
NC_000012.11:g.58143960_58143963delinsAAAT , CM000674.1:g.58143960_58143963delinsAAAT	GRCh37
NC_000012.10:g.56430227_56430230delinsAAAT	NCBI36
NG_007484.2:g.7202_7205delinsATTT , LRG_490:g.7202_7205delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+476_632+479delinsATTT (CDK4) MANE Select	ENSP00000257904.5:n.632+476_632+479delinsATTT
ENST00000257910.8:c.*2887_*2890delinsAAAT (TSPAN31) MANE Select	ENSP00000257910.3:n.*2887_*2890delinsAAAT
ENST00000257904.10:c.632+476_632+479delinsATTT (CDK4)	ENSP00000257904.5:n.632+476_632+479delinsATTT
ENST00000312990.10:c.280+476_280+479delinsATTT (CDK4)	ENSP00000316889.6:n.280+476_280+479delinsATTT
ENST00000546489.5:c.410+476_410+479delinsATTT (CDK4)	ENSP00000447779.1:n.410+476_410+479delinsATTT
ENST00000547281.5:c.410+476_410+479delinsATTT (CDK4)	ENSP00000447274.1:n.410+476_410+479delinsATTT
ENST00000547992.5:c.*2887_*2890delinsAAAT (TSPAN31)	ENSP00000448209.1:n.*2887_*2890delinsAAAT
ENST00000549606.5:c.-157-676_-157-673delinsATTT (CDK4)	ENSP00000447005.1:n.-157-676_-157-673delinsATTT
ENST00000550419.5:c.*38+262_*38+265delinsATTT (CDK4)	ENSP00000448098.1:n.*38+262_*38+265delinsATTT
ENST00000551888.5:n.458+476_458+479delinsATTT (CDK4)
ENST00000553237.5:c.*271+476_*271+479delinsATTT (CDK4)	ENSP00000448885.1:n.*271+476_*271+479delinsATTT
NM_000075.3:c.632+476_632+479delinsATTT (CDK4)	NP_000066.1:n.632+476_632+479delinsATTT
NM_000075.4:c.632+476_632+479delinsATTT (CDK4) MANE Select	NP_000066.1:n.632+476_632+479delinsATTT
NM_005981.5:c.*2887_*2890delinsAAAT (TSPAN31) MANE Select	NP_005972.1:n.*2887_*2890delinsAAAT
NM_001330168.2:c.*2887_*2890delinsAAAT (TSPAN31)	NP_001317097.1:n.*2887_*2890delinsAAAT
NM_001330169.2:c.*2887_*2890delinsAAAT (TSPAN31)	NP_001317098.1:n.*2887_*2890delinsAAAT