Canonical Allele Identifier: CA1097031980
Gene: CCR6 HGNC NCBI

Linked Data

dbSNP Id: rs1781554521

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167119516_167119517del , CM000668.2:g.167119516_167119517del GRCh38
NC_000006.11:g.167533004_167533005del , CM000668.1:g.167533004_167533005del GRCh37
NC_000006.10:g.167452994_167452995del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609590.2:n.2170-15418_2170-15417del
ENST00000705249.1:c.1066-16522_1066-16521del ENSP00000516101.1:n.1066-16522_1066-16521del
ENST00000705250.1:c.844-16522_844-16521del ENSP00000516102.1:n.844-16522_844-16521del
ENST00000705251.1:c.*713-16522_*713-16521del ENSP00000516103.1:n.*713-16522_*713-16521del
ENST00000705252.1:c.*536-16522_*536-16521del ENSP00000516104.1:n.*536-16522_*536-16521del
ENST00000705253.1:c.*536-16522_*536-16521del ENSP00000516105.1:n.*536-16522_*536-16521del
ENST00000705254.1:c.673-16522_673-16521del ENSP00000516106.1:n.673-16522_673-16521del
ENST00000705255.1:n.1692-16522_1692-16521del
ENST00000400926.5:c.-98+7502_-98+7503del ENSP00000383715.2:n.-98+7502_-98+7503del
NM_004367.5:c.-98+7502_-98+7503del NP_004358.2:n.-98+7502_-98+7503del
XR_943250.1:n.3078_3079del
XR_943251.1:n.3078_3079del
XR_001744467.2:n.1188-175_1188-174del
XR_001744469.2:n.1118-175_1118-174del
XR_943250.3:n.2845_2846del
XR_943251.3:n.3086_3087del
NM_004367.6:c.-98+7502_-98+7503del NP_004358.2:n.-98+7502_-98+7503del