Canonical Allele Identifier: CA2038997445

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751726C= , CM000674.2:g.57751726C=	GRCh38
NC_000012.11:g.58145509C= , CM000674.1:g.58145509C=	GRCh37
NC_000012.10:g.56431776C=	NCBI36
NG_007484.2:g.5656G= , LRG_490:g.5656G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.-9G= MANE Select	ENSP00000257904.5:n.-9G=
ENST00000257904.10:c.-9G=	ENSP00000257904.5:n.-9G=
ENST00000312990.10:c.-9G=	ENSP00000316889.6:n.-9G=
ENST00000546489.5:c.-4-384G=	ENSP00000447779.1:n.-4-384G=
ENST00000547281.5:c.-164-67G=	ENSP00000447274.1:n.-164-67G=
ENST00000547853.1:c.-9G=	ENSP00000449725.1:n.-9G=
ENST00000549606.5:c.-158+449G=	ENSP00000447005.1:n.-158+449G=
ENST00000550419.5:c.-9G=	ENSP00000448098.1:n.-9G=
ENST00000551706.1:n.201G=
ENST00000551800.5:c.-201-30G=	ENSP00000449391.1:n.-201-30G=
ENST00000551888.5:n.170G=
ENST00000552254.5:c.-9G=	ENSP00000449179.1:n.-9G=
ENST00000552388.1:c.-9G=	ENSP00000448963.1:n.-9G=
ENST00000552862.1:c.-9G=	ENSP00000446763.1:n.-9G=
ENST00000553237.5:c.-9G=	ENSP00000448885.1:n.-9G=
NM_000075.3:c.-9G=	NP_000066.1:n.-9G=
NM_000075.4:c.-9G= MANE Select	NP_000066.1:n.-9G=