Canonical Allele Identifier: CA2038997442

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751724A= , CM000674.2:g.57751724A=	GRCh38
NC_000012.11:g.58145507A= , CM000674.1:g.58145507A=	GRCh37
NC_000012.10:g.56431774A=	NCBI36
NG_007484.2:g.5658T= , LRG_490:g.5658T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.-7T= MANE Select	ENSP00000257904.5:n.-7T=
ENST00000257904.10:c.-7T=	ENSP00000257904.5:n.-7T=
ENST00000312990.10:c.-7T=	ENSP00000316889.6:n.-7T=
ENST00000546489.5:c.-4-382T=	ENSP00000447779.1:n.-4-382T=
ENST00000547281.5:c.-164-65T=	ENSP00000447274.1:n.-164-65T=
ENST00000547853.1:c.-7T=	ENSP00000449725.1:n.-7T=
ENST00000549606.5:c.-158+451T=	ENSP00000447005.1:n.-158+451T=
ENST00000550419.5:c.-7T=	ENSP00000448098.1:n.-7T=
ENST00000551706.1:n.203T=
ENST00000551800.5:c.-201-28T=	ENSP00000449391.1:n.-201-28T=
ENST00000551888.5:n.172T=
ENST00000552254.5:c.-7T=	ENSP00000449179.1:n.-7T=
ENST00000552388.1:c.-7T=	ENSP00000448963.1:n.-7T=
ENST00000552862.1:c.-7T=	ENSP00000446763.1:n.-7T=
ENST00000553237.5:c.-7T=	ENSP00000448885.1:n.-7T=
NM_000075.3:c.-7T=	NP_000066.1:n.-7T=
NM_000075.4:c.-7T= MANE Select	NP_000066.1:n.-7T=