Canonical Allele Identifier: CA2681199633

Gene: CCR6

Linked Data

• gnomAD v4: 6-167127250-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167127255del , CM000668.2:g.167127255del	GRCh38
NC_000006.11:g.167540743del , CM000668.1:g.167540743del	GRCh37
NC_000006.10:g.167460733del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-7679del
ENST00000705249.1:c.1066-8783del	ENSP00000516101.1:n.1066-8783del
ENST00000705250.1:c.844-8783del	ENSP00000516102.1:n.844-8783del
ENST00000705251.1:c.*713-8783del	ENSP00000516103.1:n.*713-8783del
ENST00000705252.1:c.*536-8783del	ENSP00000516104.1:n.*536-8783del
ENST00000705253.1:c.*536-8783del	ENSP00000516105.1:n.*536-8783del
ENST00000705254.1:c.673-8783del	ENSP00000516106.1:n.673-8783del
ENST00000705255.1:n.1692-8783del
ENST00000341935.10:c.-98+4032del MANE Select	ENSP00000343952.5:n.-98+4032del
ENST00000643861.1:c.-98+4032del	ENSP00000493637.1:n.-98+4032del
ENST00000341935.9:c.-98+4032del	ENSP00000343952.5:n.-98+4032del
ENST00000349984.6:c.-98+4032del	ENSP00000339393.4:n.-98+4032del
ENST00000400926.5:c.-97-8783del	ENSP00000383715.2:n.-97-8783del
NM_004367.5:c.-97-8783del	NP_004358.2:n.-97-8783del
NM_031409.3:c.-98+4032del	NP_113597.2:n.-98+4032del
XR_001744470.1:n.1370del
NM_004367.6:c.-97-8783del	NP_004358.2:n.-97-8783del
NM_031409.4:c.-98+4032del MANE Select	NP_113597.2:n.-98+4032del
NM_001394582.1:c.-98+4032del	NP_001381511.1:n.-98+4032del