Canonical Allele Identifier: CA1680259059
Gene: CCR6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167134985C= , CM000668.2:g.167134985C= GRCh38
NC_000006.11:g.167548473C= , CM000668.1:g.167548473C= GRCh37
NC_000006.10:g.167468463C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609590.2:n.2221C=
ENST00000705249.1:c.1066-1053C= ENSP00000516101.1:n.1066-1053C=
ENST00000705250.1:c.844-1053C= ENSP00000516102.1:n.844-1053C=
ENST00000705251.1:c.*713-1053C= ENSP00000516103.1:n.*713-1053C=
ENST00000705252.1:c.*536-1053C= ENSP00000516104.1:n.*536-1053C=
ENST00000705253.1:c.*536-1053C= ENSP00000516105.1:n.*536-1053C=
ENST00000705254.1:c.673-1053C= ENSP00000516106.1:n.673-1053C=
ENST00000705255.1:n.1692-1053C=
ENST00000341935.10:c.-97-1053C= MANE Select ENSP00000343952.5:n.-97-1053C=
ENST00000643861.1:c.-97-1053C= ENSP00000493637.1:n.-97-1053C=
ENST00000341935.9:c.-97-1053C= ENSP00000343952.5:n.-97-1053C=
ENST00000349984.6:c.-97-1053C= ENSP00000339393.4:n.-97-1053C=
ENST00000400926.5:c.-97-1053C= ENSP00000383715.2:n.-97-1053C=
NM_004367.5:c.-97-1053C= NP_004358.2:n.-97-1053C=
NM_031409.3:c.-97-1053C= NP_113597.2:n.-97-1053C=
NM_004367.6:c.-97-1053C= NP_004358.2:n.-97-1053C=
NM_031409.4:c.-97-1053C= MANE Select NP_113597.2:n.-97-1053C=
NM_001394582.1:c.-97-1053C= NP_001381511.1:n.-97-1053C=