Canonical Allele Identifier: CA2843443622

Gene: CLCN7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1460766C>A , CM000678.2:g.1460766C>A	GRCh38
NC_000016.9:g.1510767C>A , CM000678.1:g.1510767C>A	GRCh37
NC_000016.8:g.1450768C>A	NCBI36
NG_007567.1:g.19319G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.484+50G>T	ENSP00000514703.1:n.484+50G>T
ENST00000699948.1:c.484+50G>T	ENSP00000514704.1:n.484+50G>T
ENST00000699950.1:n.436+50G>T
ENST00000382745.9:c.484+50G>T MANE Select	ENSP00000372193.4:n.484+50G>T
ENST00000262318.12:c.412+50G>T	ENSP00000262318.8:n.412+50G>T
ENST00000382745.8:c.484+50G>T	ENSP00000372193.4:n.484+50G>T
ENST00000448525.5:c.412+50G>T	ENSP00000410907.1:n.412+50G>T
ENST00000569851.6:c.310+50G>T	ENSP00000461009.1:n.310+50G>T
NM_001114331.2:c.412+50G>T	NP_001107803.1:n.412+50G>T
NM_001287.5:c.484+50G>T	NP_001278.1:n.484+50G>T
XM_011522354.1:c.310+50G>T	XP_011520656.1:n.310+50G>T
NM_001287.6:c.484+50G>T MANE Select	NP_001278.1:n.484+50G>T
NM_001114331.3:c.412+50G>T	NP_001107803.1:n.412+50G>T