Canonical Allele Identifier: CA161978470

Gene: CDK6

Linked Data

• dbSNP Id: rs1044725054
• gnomAD v2: 7-92264490-G-GA
• gnomAD v3: 7-92635176-G-GA
• gnomAD v4: 7-92635176-G-GA
• MyVariant Identifiers: chr7:g.92264490_92264491insA (hg19) ; chr7:g.92635176_92635177insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92635183dup , CM000669.2:g.92635183dup	GRCh38
NC_000007.13:g.92264497dup , CM000669.1:g.92264497dup	GRCh37
NC_000007.12:g.92102433dup	NCBI36
NG_015888.1:g.206451dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424848.3:c.648-12091dup MANE Select	ENSP00000397087.3:n.648-12091dup
ENST00000265734.8:c.648-12091dup	ENSP00000265734.4:n.648-12091dup
ENST00000424848.2:c.648-12091dup	ENSP00000397087.2:n.648-12091dup
NM_001145306.1:c.648-12091dup	NP_001138778.1:n.648-12091dup
NM_001259.6:c.648-12091dup	NP_001250.1:n.648-12091dup
XM_006715835.1:c.648-12091dup	XP_006715898.1:n.648-12091dup
XM_011515731.1:c.648-12091dup	XP_011514033.1:n.648-12091dup
XR_927748.1:n.465-6776dup
NM_001259.7:c.648-12091dup	NP_001250.1:n.648-12091dup
XM_006715835.2:c.648-12091dup	XP_006715898.1:n.648-12091dup
XR_002956577.1:n.6999dup
XR_002956578.1:n.4647dup
NM_001145306.2:c.648-12091dup MANE Select	NP_001138778.1:n.648-12091dup
NM_001259.8:c.648-12091dup	NP_001250.1:n.648-12091dup