Canonical Allele Identifier: CA2038996971
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs1759356923

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57751458_57751459del , CM000674.2:g.57751458_57751459del GRCh38
NC_000012.11:g.58145241_58145242del , CM000674.1:g.58145241_58145242del GRCh37
NC_000012.10:g.56431508_56431509del NCBI36
NG_007484.2:g.5925_5926del , LRG_490:g.5925_5926del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.218+43_218+44del MANE Select ENSP00000257904.5:n.218+43_218+44del
ENST00000257904.10:c.218+43_218+44del ENSP00000257904.5:n.218+43_218+44del
ENST00000312990.10:c.218+43_218+44del ENSP00000316889.6:n.218+43_218+44del
ENST00000546489.5:c.-4-115_-4-114del ENSP00000447779.1:n.-4-115_-4-114del
ENST00000547281.5:c.-5+43_-5+44del ENSP00000447274.1:n.-5+43_-5+44del
ENST00000549606.5:c.-158+718_-158+719del ENSP00000447005.1:n.-158+718_-158+719del
ENST00000550419.5:c.218+43_218+44del ENSP00000448098.1:n.218+43_218+44del
ENST00000551706.1:n.470_471del
ENST00000551800.5:c.-5+43_-5+44del ENSP00000449391.1:n.-5+43_-5+44del
ENST00000551888.5:n.396+43_396+44del
ENST00000552254.5:c.218+43_218+44del ENSP00000449179.1:n.218+43_218+44del
ENST00000552388.1:c.218+43_218+44del ENSP00000448963.1:n.218+43_218+44del
ENST00000552862.1:c.218+43_218+44del ENSP00000446763.1:n.218+43_218+44del
ENST00000553237.5:c.218+43_218+44del ENSP00000448885.1:n.218+43_218+44del
NM_000075.3:c.218+43_218+44del NP_000066.1:n.218+43_218+44del
NM_000075.4:c.218+43_218+44del MANE Select NP_000066.1:n.218+43_218+44del