Canonical Allele Identifier: CA1680250450

Gene: CCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119621T= , CM000668.2:g.167119621T=	GRCh38
NC_000006.11:g.167533109T= , CM000668.1:g.167533109T=	GRCh37
NC_000006.10:g.167453099T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15313T=
ENST00000705249.1:c.1066-16417T=	ENSP00000516101.1:n.1066-16417T=
ENST00000705250.1:c.844-16417T=	ENSP00000516102.1:n.844-16417T=
ENST00000705251.1:c.*713-16417T=	ENSP00000516103.1:n.*713-16417T=
ENST00000705252.1:c.*536-16417T=	ENSP00000516104.1:n.*536-16417T=
ENST00000705253.1:c.*536-16417T=	ENSP00000516105.1:n.*536-16417T=
ENST00000705254.1:c.673-16417T=	ENSP00000516106.1:n.673-16417T=
ENST00000705255.1:n.1692-16417T=
ENST00000400926.5:c.-98+7607T=	ENSP00000383715.2:n.-98+7607T=
NM_004367.5:c.-98+7607T=	NP_004358.2:n.-98+7607T=
XR_943250.1:n.2974A=
XR_943251.1:n.2974A=
XR_001744467.2:n.1188-279A=
XR_001744469.2:n.1118-279A=
XR_943250.3:n.2741A=
XR_943251.3:n.2982A=
NM_004367.6:c.-98+7607T=	NP_004358.2:n.-98+7607T=