Canonical Allele Identifier: CA2038997254

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751599G= , CM000674.2:g.57751599G=	GRCh38
NC_000012.11:g.58145382G= , CM000674.1:g.58145382G=	GRCh37
NC_000012.10:g.56431649G=	NCBI36
NG_007484.2:g.5783C= , LRG_490:g.5783C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.119C= MANE Select	ENSP00000257904.5:p.Pro40=
ENST00000257904.10:c.119C=	ENSP00000257904.5:p.Pro40=
ENST00000312990.10:c.119C=	ENSP00000316889.6:p.Pro40=
ENST00000546489.5:c.-4-257C=	ENSP00000447779.1:n.-4-257C=
ENST00000547281.5:c.-104C=	ENSP00000447274.1:n.-104C=
ENST00000549606.5:c.-158+576C=	ENSP00000447005.1:n.-158+576C=
ENST00000550419.5:c.119C=	ENSP00000448098.1:p.Pro40=
ENST00000551706.1:n.328C=
ENST00000551800.5:c.-104C=	ENSP00000449391.1:n.-104C=
ENST00000551888.5:n.297C=
ENST00000552254.5:c.119C=	ENSP00000449179.1:p.Pro40=
ENST00000552388.1:c.119C=	ENSP00000448963.1:p.Pro40=
ENST00000552862.1:c.119C=	ENSP00000446763.1:p.Pro40=
ENST00000553237.5:c.119C=	ENSP00000448885.1:p.Pro40=
NM_000075.3:c.119C=	NP_000066.1:p.Pro40=
NM_000075.4:c.119C= MANE Select	NP_000066.1:p.Pro40=