Canonical Allele Identifier: CA1680254562

Gene: CCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167125409T= , CM000668.2:g.167125409T=	GRCh38
NC_000006.11:g.167538897T= , CM000668.1:g.167538897T=	GRCh37
NC_000006.10:g.167458887T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_031409.4:c.-98+2186T= MANE Select	NP_113597.2:n.-98+2186T=
ENST00000341935.10:c.-98+2186T= MANE Select	ENSP00000343952.5:n.-98+2186T=
NM_001394582.1:c.-98+2186T=	NP_001381511.1:n.-98+2186T=
NM_004367.5:c.-97-10629T=	NP_004358.2:n.-97-10629T=
NM_004367.6:c.-97-10629T=	NP_004358.2:n.-97-10629T=
NM_031409.3:c.-98+2186T=	NP_113597.2:n.-98+2186T=
ENST00000341935.9:c.-98+2186T=	ENSP00000343952.5:n.-98+2186T=
ENST00000349984.6:c.-98+2186T=	ENSP00000339393.4:n.-98+2186T=
ENST00000400926.5:c.-97-10629T=	ENSP00000383715.2:n.-97-10629T=
ENST00000609590.2:n.2170-9525T=
ENST00000643861.1:c.-98+2186T=	ENSP00000493637.1:n.-98+2186T=
ENST00000705249.1:c.1066-10629T=	ENSP00000516101.1:n.1066-10629T=
ENST00000705250.1:c.844-10629T=	ENSP00000516102.1:n.844-10629T=
ENST00000705251.1:c.*713-10629T=	ENSP00000516103.1:n.*713-10629T=
ENST00000705252.1:c.*536-10629T=	ENSP00000516104.1:n.*536-10629T=
ENST00000705253.1:c.*536-10629T=	ENSP00000516105.1:n.*536-10629T=
ENST00000705254.1:c.673-10629T=	ENSP00000516106.1:n.673-10629T=
ENST00000705255.1:n.1692-10629T=