Canonical Allele Identifier: CA2038995540

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750845C= , CM000674.2:g.57750845C=	GRCh38
NC_000012.11:g.58144628C= , CM000674.1:g.58144628C=	GRCh37
NC_000012.10:g.56430895C=	NCBI36
NG_007484.2:g.6537G= , LRG_490:g.6537G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.522+78G= MANE Select	ENSP00000257904.5:n.522+78G=
ENST00000257904.10:c.522+78G=	ENSP00000257904.5:n.522+78G=
ENST00000312990.10:c.265-174G=	ENSP00000316889.6:n.265-174G=
ENST00000546489.5:c.300+78G=	ENSP00000447779.1:n.300+78G=
ENST00000547281.5:c.300+78G=	ENSP00000447274.1:n.300+78G=
ENST00000549606.5:c.-158+1330G=	ENSP00000447005.1:n.-158+1330G=
ENST00000550419.5:c.522+78G=	ENSP00000448098.1:n.522+78G=
ENST00000551706.1:n.966G=
ENST00000551800.5:c.300+78G=	ENSP00000449391.1:n.300+78G=
ENST00000551888.5:n.443-174G=
ENST00000552254.5:c.522+78G=	ENSP00000449179.1:n.522+78G=
ENST00000553237.5:c.*161+78G=	ENSP00000448885.1:n.*161+78G=
NM_000075.3:c.522+78G=	NP_000066.1:n.522+78G=
NM_000075.4:c.522+78G= MANE Select	NP_000066.1:n.522+78G=