Canonical Allele Identifier: CA2038994810
Gene: CDK4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750566_57750567delinsCA , CM000674.2:g.57750566_57750567delinsCA GRCh38
NC_000012.11:g.58144349_58144350delinsCA , CM000674.1:g.58144349_58144350delinsCA GRCh37
NC_000012.10:g.56430616_56430617delinsCA NCBI36
NG_007484.2:g.6815_6816delinsTG , LRG_490:g.6815_6816delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.632+89_632+90delinsTG MANE Select ENSP00000257904.5:n.632+89_632+90delinsTG...
ENST00000257904.10:c.632+89_632+90delinsTG ENSP00000257904.5:n.632+89_632+90delinsTG...
ENST00000312990.10:c.280+89_280+90delinsTG ENSP00000316889.6:n.280+89_280+90delinsTG...
ENST00000546489.5:c.410+89_410+90delinsTG ENSP00000447779.1:n.410+89_410+90delinsTG...
ENST00000547281.5:c.410+89_410+90delinsTG ENSP00000447274.1:n.410+89_410+90delinsTG...
ENST00000549606.5:c.-157-1063_-157-1062delinsTG ENSP00000447005.1:n.-157-1063_-157-1062de...
ENST00000550419.5:c.523-4_523-3delinsTG ENSP00000448098.1:n.523-4_523-3delinsTG
ENST00000551888.5:n.458+89_458+90delinsTG
ENST00000553237.5:c.*271+89_*271+90delinsTG ENSP00000448885.1:n.*271+89_*271+90delins...
NM_000075.3:c.632+89_632+90delinsTG NP_000066.1:n.632+89_632+90delinsTG
NM_000075.4:c.632+89_632+90delinsTG MANE Select NP_000066.1:n.632+89_632+90delinsTG
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