Canonical Allele Identifier: CA843873028

Gene: CDK6

Linked Data

• dbSNP Id: rs1364086766
• gnomAD v3: 7-92635173-TG-T
• gnomAD v4: 7-92635173-TG-T
• MyVariant Identifiers: chr7:g.92264488del (hg19) ; chr7:g.92635174del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92635176del , CM000669.2:g.92635176del	GRCh38
NC_000007.13:g.92264490del , CM000669.1:g.92264490del	GRCh37
NC_000007.12:g.92102426del	NCBI36
NG_015888.1:g.206454del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424848.3:c.648-12088del MANE Select	ENSP00000397087.3:n.648-12088del
ENST00000265734.8:c.648-12088del	ENSP00000265734.4:n.648-12088del
ENST00000424848.2:c.648-12088del	ENSP00000397087.2:n.648-12088del
NM_001145306.1:c.648-12088del	NP_001138778.1:n.648-12088del
NM_001259.6:c.648-12088del	NP_001250.1:n.648-12088del
XM_006715835.1:c.648-12088del	XP_006715898.1:n.648-12088del
XM_011515731.1:c.648-12088del	XP_011514033.1:n.648-12088del
XR_927748.1:n.465-6783del
NM_001259.7:c.648-12088del	NP_001250.1:n.648-12088del
XM_006715835.2:c.648-12088del	XP_006715898.1:n.648-12088del
XR_002956577.1:n.7002del
XR_002956578.1:n.4650del
NM_001145306.2:c.648-12088del MANE Select	NP_001138778.1:n.648-12088del
NM_001259.8:c.648-12088del	NP_001250.1:n.648-12088del