Canonical Allele Identifier: CA1680259019
Gene: CCR6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167134884_167134887delinsAAAG , CM000668.2:g.167134884_167134887delinsAAAG GRCh38
NC_000006.11:g.167548372_167548375delinsAAAG , CM000668.1:g.167548372_167548375delinsAAAG GRCh37
NC_000006.10:g.167468362_167468365delinsAAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609590.2:n.2170-50_2170-47delinsAAAG
ENST00000705249.1:c.1066-1154_1066-1151delinsAAAG ENSP00000516101.1:n.1066-1154_1066-1151delinsAAAG
ENST00000705250.1:c.844-1154_844-1151delinsAAAG ENSP00000516102.1:n.844-1154_844-1151delinsAAAG
ENST00000705251.1:c.*713-1154_*713-1151delinsAAAG ENSP00000516103.1:n.*713-1154_*713-1151delinsAAAG
ENST00000705252.1:c.*536-1154_*536-1151delinsAAAG ENSP00000516104.1:n.*536-1154_*536-1151delinsAAAG
ENST00000705253.1:c.*536-1154_*536-1151delinsAAAG ENSP00000516105.1:n.*536-1154_*536-1151delinsAAAG
ENST00000705254.1:c.673-1154_673-1151delinsAAAG ENSP00000516106.1:n.673-1154_673-1151delinsAAAG
ENST00000705255.1:n.1692-1154_1692-1151delinsAAAG
ENST00000341935.10:c.-97-1154_-97-1151delinsAAAG MANE Select ENSP00000343952.5:n.-97-1154_-97-1151delinsAAAG
ENST00000643861.1:c.-97-1154_-97-1151delinsAAAG ENSP00000493637.1:n.-97-1154_-97-1151delinsAAAG
ENST00000341935.9:c.-97-1154_-97-1151delinsAAAG ENSP00000343952.5:n.-97-1154_-97-1151delinsAAAG
ENST00000349984.6:c.-97-1154_-97-1151delinsAAAG ENSP00000339393.4:n.-97-1154_-97-1151delinsAAAG
ENST00000400926.5:c.-97-1154_-97-1151delinsAAAG ENSP00000383715.2:n.-97-1154_-97-1151delinsAAAG
NM_004367.5:c.-97-1154_-97-1151delinsAAAG NP_004358.2:n.-97-1154_-97-1151delinsAAAG
NM_031409.3:c.-97-1154_-97-1151delinsAAAG NP_113597.2:n.-97-1154_-97-1151delinsAAAG
NM_004367.6:c.-97-1154_-97-1151delinsAAAG NP_004358.2:n.-97-1154_-97-1151delinsAAAG
NM_031409.4:c.-97-1154_-97-1151delinsAAAG MANE Select NP_113597.2:n.-97-1154_-97-1151delinsAAAG
NM_001394582.1:c.-97-1154_-97-1151delinsAAAG NP_001381511.1:n.-97-1154_-97-1151delinsAAAG