Canonical Allele Identifier: CA2038996887

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751352G= , CM000674.2:g.57751352G=	GRCh38
NC_000012.11:g.58145135G= , CM000674.1:g.58145135G=	GRCh37
NC_000012.10:g.56431402G=	NCBI36
NG_007484.2:g.6030C= , LRG_490:g.6030C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.219-10C= MANE Select	ENSP00000257904.5:n.219-10C=
ENST00000257904.10:c.219-10C=	ENSP00000257904.5:n.219-10C=
ENST00000312990.10:c.219-10C=	ENSP00000316889.6:n.219-10C=
ENST00000546489.5:c.-4-10C=	ENSP00000447779.1:n.-4-10C=
ENST00000547281.5:c.-4-10C=	ENSP00000447274.1:n.-4-10C=
ENST00000549606.5:c.-158+823C=	ENSP00000447005.1:n.-158+823C=
ENST00000550419.5:c.219-10C=	ENSP00000448098.1:n.219-10C=
ENST00000551706.1:n.575C=
ENST00000551800.5:c.-4-10C=	ENSP00000449391.1:n.-4-10C=
ENST00000551888.5:n.397-10C=
ENST00000552254.5:c.219-10C=	ENSP00000449179.1:n.219-10C=
ENST00000552388.1:c.219-10C=	ENSP00000448963.1:n.219-10C=
ENST00000552862.1:c.219-10C=	ENSP00000446763.1:n.219-10C=
ENST00000553237.5:c.218+148C=	ENSP00000448885.1:n.218+148C=
NM_000075.3:c.219-10C=	NP_000066.1:n.219-10C=
NM_000075.4:c.219-10C= MANE Select	NP_000066.1:n.219-10C=