Canonical Allele Identifier: CA2038994168
Gene: CDK4 HGNC NCBI
TSPAN31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750192_57750207delinsTAAATAAAAAATAAAG , CM000674.2:g.57750192_57750207delinsTAAATAAAAAATAAAG GRCh38
NC_000012.11:g.58143975_58143990delinsTAAATAAAAAATAAAG , CM000674.1:g.58143975_58143990delinsTAAATAAAAAATAAAG GRCh37
NC_000012.10:g.56430242_56430257delinsTAAATAAAAAATAAAG NCBI36
NG_007484.2:g.7175_7190delinsCTTTATTTTTTATTTA , LRG_490:g.7175_7190delinsCTTTATTTTTTATTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+449_632+464delinsCTTTATTTTTTATTTA (CDK4) MANE Select ENSP00000257904.5:n.632+449_632+464delinsCTTTATTTTTTATTTA
ENST00000257910.8:c.*2902_*2917delinsTAAATAAAAAATAAAG (TSPAN31) MANE Select ENSP00000257910.3:n.*2902_*2917delinsTAAATAAAAAATAAAG
ENST00000257904.10:c.632+449_632+464delinsCTTTATTTTTTATTTA (CDK4) ENSP00000257904.5:n.632+449_632+464delinsCTTTATTTTTTATTTA
ENST00000312990.10:c.280+449_280+464delinsCTTTATTTTTTATTTA (CDK4) ENSP00000316889.6:n.280+449_280+464delinsCTTTATTTTTTATTTA
ENST00000546489.5:c.410+449_410+464delinsCTTTATTTTTTATTTA (CDK4) ENSP00000447779.1:n.410+449_410+464delinsCTTTATTTTTTATTTA
ENST00000547281.5:c.410+449_410+464delinsCTTTATTTTTTATTTA (CDK4) ENSP00000447274.1:n.410+449_410+464delinsCTTTATTTTTTATTTA
ENST00000547992.5:c.*2902_*2917delinsTAAATAAAAAATAAAG (TSPAN31) ENSP00000448209.1:n.*2902_*2917delinsTAAATAAAAAATAAAG
ENST00000549606.5:c.-157-703_-157-688delinsCTTTATTTTTTATTTA (CDK4) ENSP00000447005.1:n.-157-703_-157-688delinsCTTTATTTTTTATTTA
ENST00000550419.5:c.*38+235_*38+250delinsCTTTATTTTTTATTTA (CDK4) ENSP00000448098.1:n.*38+235_*38+250delinsCTTTATTTTTTATTTA
ENST00000551888.5:n.458+449_458+464delinsCTTTATTTTTTATTTA (CDK4)
ENST00000553237.5:c.*271+449_*271+464delinsCTTTATTTTTTATTTA (CDK4) ENSP00000448885.1:n.*271+449_*271+464delinsCTTTATTTTTTATTTA
NM_000075.3:c.632+449_632+464delinsCTTTATTTTTTATTTA (CDK4) NP_000066.1:n.632+449_632+464delinsCTTTATTTTTTATTTA
NM_000075.4:c.632+449_632+464delinsCTTTATTTTTTATTTA (CDK4) MANE Select NP_000066.1:n.632+449_632+464delinsCTTTATTTTTTATTTA
NM_005981.5:c.*2902_*2917delinsTAAATAAAAAATAAAG (TSPAN31) MANE Select NP_005972.1:n.*2902_*2917delinsTAAATAAAAAATAAAG
NM_001330168.2:c.*2902_*2917delinsTAAATAAAAAATAAAG (TSPAN31) NP_001317097.1:n.*2902_*2917delinsTAAATAAAAAATAAAG
NM_001330169.2:c.*2902_*2917delinsTAAATAAAAAATAAAG (TSPAN31) NP_001317098.1:n.*2902_*2917delinsTAAATAAAAAATAAAG