Canonical Allele Identifier: CA1725977829
Gene: CDK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92634925A= , CM000669.2:g.92634925A= GRCh38
NC_000007.13:g.92264239A= , CM000669.1:g.92264239A= GRCh37
NC_000007.12:g.92102175A= NCBI36
NG_015888.1:g.206703T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000424848.3:c.648-11839T= MANE Select ENSP00000397087.3:n.648-11839T=
ENST00000265734.8:c.648-11839T= ENSP00000265734.4:n.648-11839T=
ENST00000424848.2:c.648-11839T= ENSP00000397087.2:n.648-11839T=
NM_001145306.1:c.648-11839T= NP_001138778.1:n.648-11839T=
NM_001259.6:c.648-11839T= NP_001250.1:n.648-11839T=
XM_006715835.1:c.648-11839T= XP_006715898.1:n.648-11839T=
XM_011515731.1:c.648-11839T= XP_011514033.1:n.648-11839T=
XR_927748.1:n.465-7034A=
NM_001259.7:c.648-11839T= NP_001250.1:n.648-11839T=
XM_006715835.2:c.648-11839T= XP_006715898.1:n.648-11839T=
XR_002956577.1:n.7251T=
XR_002956578.1:n.4899T=
NM_001145306.2:c.648-11839T= MANE Select NP_001138778.1:n.648-11839T=
NM_001259.8:c.648-11839T= NP_001250.1:n.648-11839T=