Canonical Allele Identifier: CA1680249823

Gene: CCR6

Linked Data

• dbSNP Id: rs1781548522

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119231_167119234del , CM000668.2:g.167119231_167119234del	GRCh38
NC_000006.11:g.167532719_167532722del , CM000668.1:g.167532719_167532722del	GRCh37
NC_000006.10:g.167452709_167452712del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-15703_2170-15700del
ENST00000705249.1:c.1066-16807_1066-16804del	ENSP00000516101.1:n.1066-16807_1066-16804del
ENST00000705250.1:c.844-16807_844-16804del	ENSP00000516102.1:n.844-16807_844-16804del
ENST00000705251.1:c.*713-16807_*713-16804del	ENSP00000516103.1:n.*713-16807_*713-16804del
ENST00000705252.1:c.*536-16807_*536-16804del	ENSP00000516104.1:n.*536-16807_*536-16804del
ENST00000705253.1:c.*536-16807_*536-16804del	ENSP00000516105.1:n.*536-16807_*536-16804del
ENST00000705254.1:c.673-16807_673-16804del	ENSP00000516106.1:n.673-16807_673-16804del
ENST00000705255.1:n.1692-16807_1692-16804del
ENST00000400926.5:c.-98+7217_-98+7220del	ENSP00000383715.2:n.-98+7217_-98+7220del
NM_004367.5:c.-98+7217_-98+7220del	NP_004358.2:n.-98+7217_-98+7220del
XR_943250.1:n.3362_3365del
XR_943251.1:n.3362_3365del
XR_001744467.2:n.1297_1300del
XR_001744469.2:n.1227_1230del
XR_943250.3:n.3129_3132del
XR_943251.3:n.3370_3373del
NM_004367.6:c.-98+7217_-98+7220del	NP_004358.2:n.-98+7217_-98+7220del