Canonical Allele Identifier: CA1680250584

Gene: CCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119756_167119757delinsCT , CM000668.2:g.167119756_167119757delinsCT	GRCh38
NC_000006.11:g.167533244_167533245delinsCT , CM000668.1:g.167533244_167533245delinsCT	GRCh37
NC_000006.10:g.167453234_167453235delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15178_2170-15177delinsCT
ENST00000705249.1:c.1066-16282_1066-16281delinsCT	ENSP00000516101.1:n.1066-16282_1066-16281delinsCT
ENST00000705250.1:c.844-16282_844-16281delinsCT	ENSP00000516102.1:n.844-16282_844-16281delinsCT
ENST00000705251.1:c.*713-16282_*713-16281delinsCT	ENSP00000516103.1:n.*713-16282_*713-16281delinsCT
ENST00000705252.1:c.*536-16282_*536-16281delinsCT	ENSP00000516104.1:n.*536-16282_*536-16281delinsCT
ENST00000705253.1:c.*536-16282_*536-16281delinsCT	ENSP00000516105.1:n.*536-16282_*536-16281delinsCT
ENST00000705254.1:c.673-16282_673-16281delinsCT	ENSP00000516106.1:n.673-16282_673-16281delinsCT
ENST00000705255.1:n.1692-16282_1692-16281delinsCT
ENST00000400926.5:c.-98+7742_-98+7743delinsCT	ENSP00000383715.2:n.-98+7742_-98+7743delinsCT
NM_004367.5:c.-98+7742_-98+7743delinsCT	NP_004358.2:n.-98+7742_-98+7743delinsCT
XR_943250.1:n.2838_2839delinsAG
XR_943251.1:n.2838_2839delinsAG
XR_001744467.2:n.1188-415_1188-414delinsAG
XR_001744469.2:n.1118-415_1118-414delinsAG
XR_943250.3:n.2605_2606delinsAG
XR_943251.3:n.2846_2847delinsAG
NM_004367.6:c.-98+7742_-98+7743delinsCT	NP_004358.2:n.-98+7742_-98+7743delinsCT