Canonical Allele Identifier: CA1680250388

Gene: CCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119561_167119562delinsCT , CM000668.2:g.167119561_167119562delinsCT	GRCh38
NC_000006.11:g.167533049_167533050delinsCT , CM000668.1:g.167533049_167533050delinsCT	GRCh37
NC_000006.10:g.167453039_167453040delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15373_2170-15372delinsCT
ENST00000705249.1:c.1066-16477_1066-16476delinsCT	ENSP00000516101.1:n.1066-16477_1066-16476delinsCT
ENST00000705250.1:c.844-16477_844-16476delinsCT	ENSP00000516102.1:n.844-16477_844-16476delinsCT
ENST00000705251.1:c.*713-16477_*713-16476delinsCT	ENSP00000516103.1:n.*713-16477_*713-16476delinsCT
ENST00000705252.1:c.*536-16477_*536-16476delinsCT	ENSP00000516104.1:n.*536-16477_*536-16476delinsCT
ENST00000705253.1:c.*536-16477_*536-16476delinsCT	ENSP00000516105.1:n.*536-16477_*536-16476delinsCT
ENST00000705254.1:c.673-16477_673-16476delinsCT	ENSP00000516106.1:n.673-16477_673-16476delinsCT
ENST00000705255.1:n.1692-16477_1692-16476delinsCT
ENST00000400926.5:c.-98+7547_-98+7548delinsCT	ENSP00000383715.2:n.-98+7547_-98+7548delinsCT
NM_004367.5:c.-98+7547_-98+7548delinsCT	NP_004358.2:n.-98+7547_-98+7548delinsCT
XR_943250.1:n.3033_3034delinsAG
XR_943251.1:n.3033_3034delinsAG
XR_001744467.2:n.1188-220_1188-219delinsAG
XR_001744469.2:n.1118-220_1118-219delinsAG
XR_943250.3:n.2800_2801delinsAG
XR_943251.3:n.3041_3042delinsAG
NM_004367.6:c.-98+7547_-98+7548delinsCT	NP_004358.2:n.-98+7547_-98+7548delinsCT