Canonical Allele Identifier: CA1725991159
Gene: CDK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92651381T= , CM000669.2:g.92651381T= GRCh38
NC_000007.13:g.92280695T= , CM000669.1:g.92280695T= GRCh37
NC_000007.12:g.92118631T= NCBI36
NG_015888.1:g.190247A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000424848.3:c.647+20045A= MANE Select ENSP00000397087.3:n.647+20045A=
ENST00000265734.8:c.647+20045A= ENSP00000265734.4:n.647+20045A=
ENST00000424848.2:c.647+20045A= ENSP00000397087.2:n.647+20045A=
NM_001145306.1:c.647+20045A= NP_001138778.1:n.647+20045A=
NM_001259.6:c.647+20045A= NP_001250.1:n.647+20045A=
XM_006715835.1:c.647+20045A= XP_006715898.1:n.647+20045A=
XM_011515731.1:c.647+20045A= XP_011514033.1:n.647+20045A=
XR_927745.1:n.241T=
NM_001259.7:c.647+20045A= NP_001250.1:n.647+20045A=
XM_006715835.2:c.647+20045A= XP_006715898.1:n.647+20045A=
NM_001145306.2:c.647+20045A= MANE Select NP_001138778.1:n.647+20045A=
NM_001259.8:c.647+20045A= NP_001250.1:n.647+20045A=