Canonical Allele Identifier: CA2038996970
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57751455_57751457delinsCTT , CM000674.2:g.57751455_57751457delinsCTT GRCh38
NC_000012.11:g.58145238_58145240delinsCTT , CM000674.1:g.58145238_58145240delinsCTT GRCh37
NC_000012.10:g.56431505_56431507delinsCTT NCBI36
NG_007484.2:g.5925_5927delinsAAG , LRG_490:g.5925_5927delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.218+43_218+45delinsAAG MANE Select ENSP00000257904.5:n.218+43_218+45delinsAAG
ENST00000257904.10:c.218+43_218+45delinsAAG ENSP00000257904.5:n.218+43_218+45delinsAAG
ENST00000312990.10:c.218+43_218+45delinsAAG ENSP00000316889.6:n.218+43_218+45delinsAAG
ENST00000546489.5:c.-4-115_-4-113delinsAAG ENSP00000447779.1:n.-4-115_-4-113delinsAAG
ENST00000547281.5:c.-5+43_-5+45delinsAAG ENSP00000447274.1:n.-5+43_-5+45delinsAAG
ENST00000549606.5:c.-158+718_-158+720delinsAAG ENSP00000447005.1:n.-158+718_-158+720delinsAAG
ENST00000550419.5:c.218+43_218+45delinsAAG ENSP00000448098.1:n.218+43_218+45delinsAAG
ENST00000551706.1:n.470_472delinsAAG
ENST00000551800.5:c.-5+43_-5+45delinsAAG ENSP00000449391.1:n.-5+43_-5+45delinsAAG
ENST00000551888.5:n.396+43_396+45delinsAAG
ENST00000552254.5:c.218+43_218+45delinsAAG ENSP00000449179.1:n.218+43_218+45delinsAAG
ENST00000552388.1:c.218+43_218+45delinsAAG ENSP00000448963.1:n.218+43_218+45delinsAAG
ENST00000552862.1:c.218+43_218+45delinsAAG ENSP00000446763.1:n.218+43_218+45delinsAAG
ENST00000553237.5:c.218+43_218+45delinsAAG ENSP00000448885.1:n.218+43_218+45delinsAAG
NM_000075.3:c.218+43_218+45delinsAAG NP_000066.1:n.218+43_218+45delinsAAG
NM_000075.4:c.218+43_218+45delinsAAG MANE Select NP_000066.1:n.218+43_218+45delinsAAG