Canonical Allele Identifier: CA576500275

Gene: CDK6

Linked Data

• dbSNP Id: rs1445304109
• gnomAD v2: 7-92383731-CA-C
• gnomAD v3: 7-92754417-CA-C
• gnomAD v4: 7-92754417-CA-C
• MyVariant Identifiers: chr7:g.92383732del (hg19) ; chr7:g.92754418del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92754421del , CM000669.2:g.92754421del	GRCh38
NC_000007.13:g.92383735del , CM000669.1:g.92383735del	GRCh37
NC_000007.12:g.92221671del	NCBI36
NG_015888.1:g.87210del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424848.3:c.369+20278del MANE Select	ENSP00000397087.3:n.369+20278del
ENST00000265734.8:c.369+20278del	ENSP00000265734.4:n.369+20278del
ENST00000424848.2:c.369+20278del	ENSP00000397087.2:n.369+20278del
NM_001145306.1:c.369+20278del	NP_001138778.1:n.369+20278del
NM_001259.6:c.369+20278del	NP_001250.1:n.369+20278del
XM_006715835.1:c.369+20278del	XP_006715898.1:n.369+20278del
XM_006715836.2:c.369+20278del	XP_006715899.1:n.369+20278del
XM_011515731.1:c.369+20278del	XP_011514033.1:n.369+20278del
NM_001259.7:c.369+20278del	NP_001250.1:n.369+20278del
XM_006715835.2:c.369+20278del	XP_006715898.1:n.369+20278del
NM_001145306.2:c.369+20278del MANE Select	NP_001138778.1:n.369+20278del
NM_001259.8:c.369+20278del	NP_001250.1:n.369+20278del