Canonical Allele Identifier: CA2038995544

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750857A= , CM000674.2:g.57750857A=	GRCh38
NC_000012.11:g.58144640A= , CM000674.1:g.58144640A=	GRCh37
NC_000012.10:g.56430907A=	NCBI36
NG_007484.2:g.6525T= , LRG_490:g.6525T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.522+66T= MANE Select	ENSP00000257904.5:n.522+66T=
ENST00000257904.10:c.522+66T=	ENSP00000257904.5:n.522+66T=
ENST00000312990.10:c.265-186T=	ENSP00000316889.6:n.265-186T=
ENST00000546489.5:c.300+66T=	ENSP00000447779.1:n.300+66T=
ENST00000547281.5:c.300+66T=	ENSP00000447274.1:n.300+66T=
ENST00000549606.5:c.-158+1318T=	ENSP00000447005.1:n.-158+1318T=
ENST00000550419.5:c.522+66T=	ENSP00000448098.1:n.522+66T=
ENST00000551706.1:n.954T=
ENST00000551800.5:c.300+66T=	ENSP00000449391.1:n.300+66T=
ENST00000551888.5:n.443-186T=
ENST00000552254.5:c.522+66T=	ENSP00000449179.1:n.522+66T=
ENST00000553237.5:c.*161+66T=	ENSP00000448885.1:n.*161+66T=
NM_000075.3:c.522+66T=	NP_000066.1:n.522+66T=
NM_000075.4:c.522+66T= MANE Select	NP_000066.1:n.522+66T=