Canonical Allele Identifier: CA1725977884
Gene: CDK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92635013T= , CM000669.2:g.92635013T= GRCh38
NC_000007.13:g.92264327T= , CM000669.1:g.92264327T= GRCh37
NC_000007.12:g.92102263T= NCBI36
NG_015888.1:g.206615A=

Transcript Alleles

HGVS Amino-acid change
ENST00000424848.3:c.648-11927A= MANE Select ENSP00000397087.3:n.648-11927A=
ENST00000265734.8:c.648-11927A= ENSP00000265734.4:n.648-11927A=
ENST00000424848.2:c.648-11927A= ENSP00000397087.2:n.648-11927A=
NM_001145306.1:c.648-11927A= NP_001138778.1:n.648-11927A=
NM_001259.6:c.648-11927A= NP_001250.1:n.648-11927A=
XM_006715835.1:c.648-11927A= XP_006715898.1:n.648-11927A=
XM_011515731.1:c.648-11927A= XP_011514033.1:n.648-11927A=
XR_927748.1:n.465-6946T=
NM_001259.7:c.648-11927A= NP_001250.1:n.648-11927A=
XM_006715835.2:c.648-11927A= XP_006715898.1:n.648-11927A=
XR_002956577.1:n.7163A=
XR_002956578.1:n.4811A=
NM_001145306.2:c.648-11927A= MANE Select NP_001138778.1:n.648-11927A=
NM_001259.8:c.648-11927A= NP_001250.1:n.648-11927A=