Canonical Allele Identifier: CA2038995085

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750660_57750661delinsGA , CM000674.2:g.57750660_57750661delinsGA	GRCh38
NC_000012.11:g.58144443_58144444delinsGA , CM000674.1:g.58144443_58144444delinsGA	GRCh37
NC_000012.10:g.56430710_56430711delinsGA	NCBI36
NG_007484.2:g.6721_6722delinsTC , LRG_490:g.6721_6722delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.627_628delinsTC MANE Select	ENSP00000257904.5:p.Arg209=
ENST00000257904.10:c.627_628delinsTC	ENSP00000257904.5:p.Arg209=
ENST00000312990.10:c.275_276delinsTC	ENSP00000316889.6:p.Val92=
ENST00000546489.5:c.405_406delinsTC	ENSP00000447779.1:p.Arg135=
ENST00000547281.5:c.405_406delinsTC	ENSP00000447274.1:p.Arg135=
ENST00000549606.5:c.-157-1157_-157-1156delinsTC	ENSP00000447005.1:n.-157-1157_-157-1156delinsTC
ENST00000550419.5:c.523-98_523-97delinsTC	ENSP00000448098.1:n.523-98_523-97delinsTC
ENST00000551888.5:n.453_454delinsTC
ENST00000553237.5:c.*266_*267delinsTC	ENSP00000448885.1:n.*266_*267delinsTC
NM_000075.3:c.627_628delinsTC	NP_000066.1:p.Arg209=
NM_000075.4:c.627_628delinsTC MANE Select	NP_000066.1:p.Arg209=