Canonical Allele Identifier: CA1680250245

Gene: CCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119434_167119435delinsCT , CM000668.2:g.167119434_167119435delinsCT	GRCh38
NC_000006.11:g.167532922_167532923delinsCT , CM000668.1:g.167532922_167532923delinsCT	GRCh37
NC_000006.10:g.167452912_167452913delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15500_2170-15499delinsCT
ENST00000705249.1:c.1066-16604_1066-16603delinsCT	ENSP00000516101.1:n.1066-16604_1066-16603delinsCT
ENST00000705250.1:c.844-16604_844-16603delinsCT	ENSP00000516102.1:n.844-16604_844-16603delinsCT
ENST00000705251.1:c.*713-16604_*713-16603delinsCT	ENSP00000516103.1:n.*713-16604_*713-16603delinsCT
ENST00000705252.1:c.*536-16604_*536-16603delinsCT	ENSP00000516104.1:n.*536-16604_*536-16603delinsCT
ENST00000705253.1:c.*536-16604_*536-16603delinsCT	ENSP00000516105.1:n.*536-16604_*536-16603delinsCT
ENST00000705254.1:c.673-16604_673-16603delinsCT	ENSP00000516106.1:n.673-16604_673-16603delinsCT
ENST00000705255.1:n.1692-16604_1692-16603delinsCT
ENST00000400926.5:c.-98+7420_-98+7421delinsCT	ENSP00000383715.2:n.-98+7420_-98+7421delinsCT
NM_004367.5:c.-98+7420_-98+7421delinsCT	NP_004358.2:n.-98+7420_-98+7421delinsCT
XR_943250.1:n.3160_3161delinsAG
XR_943251.1:n.3160_3161delinsAG
XR_001744467.2:n.1188-93_1188-92delinsAG
XR_001744469.2:n.1118-93_1118-92delinsAG
XR_943250.3:n.2927_2928delinsAG
XR_943251.3:n.3168_3169delinsAG
NM_004367.6:c.-98+7420_-98+7421delinsCT	NP_004358.2:n.-98+7420_-98+7421delinsCT