Canonical Allele Identifier: CA2538382013
Gene: CDK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92754711C>A , CM000669.2:g.92754711C>A GRCh38
NC_000007.13:g.92384025C>A , CM000669.1:g.92384025C>A GRCh37
NC_000007.12:g.92221961C>A NCBI36
NG_015888.1:g.86917G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000424848.3:c.369+19985G>T MANE Select ENSP00000397087.3:n.369+19985G>T
ENST00000265734.8:c.369+19985G>T ENSP00000265734.4:n.369+19985G>T
ENST00000424848.2:c.369+19985G>T ENSP00000397087.2:n.369+19985G>T
NM_001145306.1:c.369+19985G>T NP_001138778.1:n.369+19985G>T
NM_001259.6:c.369+19985G>T NP_001250.1:n.369+19985G>T
XM_006715835.1:c.369+19985G>T XP_006715898.1:n.369+19985G>T
XM_006715836.2:c.369+19985G>T XP_006715899.1:n.369+19985G>T
XM_011515731.1:c.369+19985G>T XP_011514033.1:n.369+19985G>T
NM_001259.7:c.369+19985G>T NP_001250.1:n.369+19985G>T
XM_006715835.2:c.369+19985G>T XP_006715898.1:n.369+19985G>T
NM_001145306.2:c.369+19985G>T MANE Select NP_001138778.1:n.369+19985G>T
NM_001259.8:c.369+19985G>T NP_001250.1:n.369+19985G>T