Canonical Allele Identifier: CA1680259102
Gene: CCR6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167135090A= , CM000668.2:g.167135090A= GRCh38
NC_000006.11:g.167548578A= , CM000668.1:g.167548578A= GRCh37
NC_000006.10:g.167468568A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609590.2:n.2302+24A=
ENST00000705249.1:c.1066-948A= ENSP00000516101.1:n.1066-948A=
ENST00000705250.1:c.844-948A= ENSP00000516102.1:n.844-948A=
ENST00000705251.1:c.*713-948A= ENSP00000516103.1:n.*713-948A=
ENST00000705252.1:c.*536-948A= ENSP00000516104.1:n.*536-948A=
ENST00000705253.1:c.*536-948A= ENSP00000516105.1:n.*536-948A=
ENST00000705254.1:c.673-948A= ENSP00000516106.1:n.673-948A=
ENST00000705255.1:n.1692-948A=
ENST00000341935.10:c.-97-948A= MANE Select ENSP00000343952.5:n.-97-948A=
ENST00000643861.1:c.-97-948A= ENSP00000493637.1:n.-97-948A=
ENST00000341935.9:c.-97-948A= ENSP00000343952.5:n.-97-948A=
ENST00000349984.6:c.-97-948A= ENSP00000339393.4:n.-97-948A=
ENST00000400926.5:c.-97-948A= ENSP00000383715.2:n.-97-948A=
NM_004367.5:c.-97-948A= NP_004358.2:n.-97-948A=
NM_031409.3:c.-97-948A= NP_113597.2:n.-97-948A=
NM_004367.6:c.-97-948A= NP_004358.2:n.-97-948A=
NM_031409.4:c.-97-948A= MANE Select NP_113597.2:n.-97-948A=
NM_001394582.1:c.-97-948A= NP_001381511.1:n.-97-948A=