Canonical Allele Identifier: CA822270385

Gene: CCR6

Linked Data

• dbSNP Id: rs1303320714
• gnomAD v3: 6-167119193-G-GATCTGAGTCGCCTTCCT
• gnomAD v4: 6-167119193-G-GATCTGAGTCGCCTTCCT
• MyVariant Identifiers: chr6:g.167532681_167532682insATCTGAGTCGCCTTCCT (hg19) ; chr6:g.167119193_167119194insATCTGAGTCGCCTTCCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119194_167119210dup , CM000668.2:g.167119194_167119210dup	GRCh38
NC_000006.11:g.167532682_167532698dup , CM000668.1:g.167532682_167532698dup	GRCh37
NC_000006.10:g.167452672_167452688dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-15740_2170-15724dup
ENST00000705249.1:c.1066-16844_1066-16828dup	ENSP00000516101.1:n.1066-16844_1066-16828...
ENST00000705250.1:c.844-16844_844-16828dup	ENSP00000516102.1:n.844-16844_844-16828du...
ENST00000705251.1:c.*713-16844_*713-16828dup	ENSP00000516103.1:n.*713-16844_*713-16828...
ENST00000705252.1:c.*536-16844_*536-16828dup	ENSP00000516104.1:n.*536-16844_*536-16828...
ENST00000705253.1:c.*536-16844_*536-16828dup	ENSP00000516105.1:n.*536-16844_*536-16828...
ENST00000705254.1:c.673-16844_673-16828dup	ENSP00000516106.1:n.673-16844_673-16828du...
ENST00000705255.1:n.1692-16844_1692-16828dup
ENST00000400926.5:c.-98+7180_-98+7196dup	ENSP00000383715.2:n.-98+7180_-98+7196dup
NM_004367.5:c.-98+7180_-98+7196dup	NP_004358.2:n.-98+7180_-98+7196dup
XR_943250.1:n.3385_3401dup
XR_943251.1:n.3385_3401dup
XR_001744467.2:n.1320_1336dup
XR_001744469.2:n.1250_1266dup
XR_943250.3:n.3152_3168dup
XR_943251.3:n.3393_3409dup
NM_004367.6:c.-98+7180_-98+7196dup	NP_004358.2:n.-98+7180_-98+7196dup