Canonical Allele Identifier: CA2201647833

Gene: CLCN7

Linked Data

• dbSNP Id: rs2038702067

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1449112_1449115dup , CM000678.2:g.1449112_1449115dup	GRCh38
NC_000016.9:g.1499113_1499116dup , CM000678.1:g.1499113_1499116dup	GRCh37
NC_000016.8:g.1439114_1439117dup	NCBI36
NG_007567.1:g.30970_30973dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.1670-22_1670-19dup	ENSP00000514703.1:n.1670-22_1670-19dup
ENST00000699948.1:c.1624-22_1624-19dup	ENSP00000514704.1:n.1624-22_1624-19dup
ENST00000382745.9:c.1670-22_1670-19dup MANE Select	ENSP00000372193.4:n.1670-22_1670-19dup
ENST00000262318.12:c.1598-22_1598-19dup	ENSP00000262318.8:n.1598-22_1598-19dup
ENST00000382745.8:c.1670-22_1670-19dup	ENSP00000372193.4:n.1670-22_1670-19dup
ENST00000448525.5:c.1598-22_1598-19dup	ENSP00000410907.1:n.1598-22_1598-19dup
ENST00000563642.6:n.1739-22_1739-19dup
ENST00000565092.6:n.683_686dup
ENST00000567789.1:n.149_152dup
NM_001114331.2:c.1598-22_1598-19dup	NP_001107803.1:n.1598-22_1598-19dup
NM_001287.5:c.1670-22_1670-19dup	NP_001278.1:n.1670-22_1670-19dup
XM_011522354.1:c.1496-22_1496-19dup	XP_011520656.1:n.1496-22_1496-19dup
NM_001287.6:c.1670-22_1670-19dup MANE Select	NP_001278.1:n.1670-22_1670-19dup
NM_001114331.3:c.1598-22_1598-19dup	NP_001107803.1:n.1598-22_1598-19dup