Canonical Allele Identifier: CA1680255374
Gene: CCR6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167127320_167127324delinsTAGTG , CM000668.2:g.167127320_167127324delinsTAGTG GRCh38
NC_000006.11:g.167540808_167540812delinsTAGTG , CM000668.1:g.167540808_167540812delinsTAGTG GRCh37
NC_000006.10:g.167460798_167460802delinsTAGTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609590.2:n.2170-7614_2170-7610delinsTAGTG
ENST00000705249.1:c.1066-8718_1066-8714delinsTAGTG ENSP00000516101.1:n.1066-8718_1066-8714delinsTAGTG
ENST00000705250.1:c.844-8718_844-8714delinsTAGTG ENSP00000516102.1:n.844-8718_844-8714delinsTAGTG
ENST00000705251.1:c.*713-8718_*713-8714delinsTAGTG ENSP00000516103.1:n.*713-8718_*713-8714delinsTAGTG
ENST00000705252.1:c.*536-8718_*536-8714delinsTAGTG ENSP00000516104.1:n.*536-8718_*536-8714delinsTAGTG
ENST00000705253.1:c.*536-8718_*536-8714delinsTAGTG ENSP00000516105.1:n.*536-8718_*536-8714delinsTAGTG
ENST00000705254.1:c.673-8718_673-8714delinsTAGTG ENSP00000516106.1:n.673-8718_673-8714delinsTAGTG
ENST00000705255.1:n.1692-8718_1692-8714delinsTAGTG
ENST00000341935.10:c.-98+4097_-98+4101delinsTAGTG MANE Select ENSP00000343952.5:n.-98+4097_-98+4101delinsTAGTG
ENST00000643861.1:c.-98+4097_-98+4101delinsTAGTG ENSP00000493637.1:n.-98+4097_-98+4101delinsTAGTG
ENST00000341935.9:c.-98+4097_-98+4101delinsTAGTG ENSP00000343952.5:n.-98+4097_-98+4101delinsTAGTG
ENST00000349984.6:c.-98+4097_-98+4101delinsTAGTG ENSP00000339393.4:n.-98+4097_-98+4101delinsTAGTG
ENST00000400926.5:c.-97-8718_-97-8714delinsTAGTG ENSP00000383715.2:n.-97-8718_-97-8714delinsTAGTG
NM_004367.5:c.-97-8718_-97-8714delinsTAGTG NP_004358.2:n.-97-8718_-97-8714delinsTAGTG
NM_031409.3:c.-98+4097_-98+4101delinsTAGTG NP_113597.2:n.-98+4097_-98+4101delinsTAGTG
XR_001744470.1:n.1297_1301delinsCACTA
NM_004367.6:c.-97-8718_-97-8714delinsTAGTG NP_004358.2:n.-97-8718_-97-8714delinsTAGTG
NM_031409.4:c.-98+4097_-98+4101delinsTAGTG MANE Select NP_113597.2:n.-98+4097_-98+4101delinsTAGTG
NM_001394582.1:c.-98+4097_-98+4101delinsTAGTG NP_001381511.1:n.-98+4097_-98+4101delinsTAGTG