Canonical Allele Identifier: CA1726035136
Gene: CDK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92754410A= , CM000669.2:g.92754410A= GRCh38
NC_000007.13:g.92383724A= , CM000669.1:g.92383724A= GRCh37
NC_000007.12:g.92221660A= NCBI36
NG_015888.1:g.87218T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000424848.3:c.369+20286T= MANE Select ENSP00000397087.3:n.369+20286T=
ENST00000265734.8:c.369+20286T= ENSP00000265734.4:n.369+20286T=
ENST00000424848.2:c.369+20286T= ENSP00000397087.2:n.369+20286T=
NM_001145306.1:c.369+20286T= NP_001138778.1:n.369+20286T=
NM_001259.6:c.369+20286T= NP_001250.1:n.369+20286T=
XM_006715835.1:c.369+20286T= XP_006715898.1:n.369+20286T=
XM_006715836.2:c.369+20286T= XP_006715899.1:n.369+20286T=
XM_011515731.1:c.369+20286T= XP_011514033.1:n.369+20286T=
NM_001259.7:c.369+20286T= NP_001250.1:n.369+20286T=
XM_006715835.2:c.369+20286T= XP_006715898.1:n.369+20286T=
NM_001145306.2:c.369+20286T= MANE Select NP_001138778.1:n.369+20286T=
NM_001259.8:c.369+20286T= NP_001250.1:n.369+20286T=