Canonical Allele Identifier: CA2038996279

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751139C= , CM000674.2:g.57751139C=	GRCh38
NC_000012.11:g.58144922C= , CM000674.1:g.58144922C=	GRCh37
NC_000012.10:g.56431189C=	NCBI36
NG_007484.2:g.6243G= , LRG_490:g.6243G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.355-49G= MANE Select	ENSP00000257904.5:n.355-49G=
ENST00000257904.10:c.355-49G=	ENSP00000257904.5:n.355-49G=
ENST00000312990.10:c.264+158G=	ENSP00000316889.6:n.264+158G=
ENST00000546489.5:c.133-49G=	ENSP00000447779.1:n.133-49G=
ENST00000547281.5:c.133-49G=	ENSP00000447274.1:n.133-49G=
ENST00000549606.5:c.-158+1036G=	ENSP00000447005.1:n.-158+1036G=
ENST00000550419.5:c.355-49G=	ENSP00000448098.1:n.355-49G=
ENST00000551706.1:n.721-49G=
ENST00000551800.5:c.133-49G=	ENSP00000449391.1:n.133-49G=
ENST00000551888.5:n.442+158G=
ENST00000552254.5:c.355-49G=	ENSP00000449179.1:n.355-49G=
ENST00000552388.1:c.355-49G=	ENSP00000448963.1:n.355-49G=
ENST00000553237.5:c.219-49G=	ENSP00000448885.1:n.219-49G=
NM_000075.3:c.355-49G=	NP_000066.1:n.355-49G=
NM_000075.4:c.355-49G= MANE Select	NP_000066.1:n.355-49G=