Canonical Allele Identifier: CA2038997305
Community Standard Title: NM_000075.4(CDK4):c.70C= (p.Arg24=)
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57751648G= , CM000674.2:g.57751648G= GRCh38
NC_000012.11:g.58145431G= , CM000674.1:g.58145431G= GRCh37
NC_000012.10:g.56431698G= NCBI36
NG_007484.2:g.5734C= , LRG_490:g.5734C=

Transcript Alleles

HGVS Amino-acid Change
NM_000075.4:c.70C= MANE Select NP_000066.1:p.Arg24=
ENST00000257904.11:c.70C= MANE Select ENSP00000257904.5:p.Arg24=
NM_000075.3:c.70C= NP_000066.1:p.Arg24=
ENST00000257904.10:c.70C= ENSP00000257904.5:p.Arg24=
ENST00000312990.10:c.70C= ENSP00000316889.6:p.Arg24=
ENST00000546489.5:c.-4-306C= ENSP00000447779.1:n.-4-306C=
ENST00000547281.5:c.-153C= ENSP00000447274.1:n.-153C=
ENST00000549606.5:c.-158+527C= ENSP00000447005.1:n.-158+527C=
ENST00000550419.5:c.70C= ENSP00000448098.1:p.Arg24=
ENST00000551706.1:n.279C=
ENST00000551800.5:c.-153C= ENSP00000449391.1:n.-153C=
ENST00000551888.5:n.248C=
ENST00000552254.5:c.70C= ENSP00000449179.1:p.Arg24=
ENST00000552388.1:c.70C= ENSP00000448963.1:p.Arg24=
ENST00000552862.1:c.70C= ENSP00000446763.1:p.Arg24=
ENST00000553237.5:c.70C= ENSP00000448885.1:p.Arg24=