Canonical Allele Identifier: CA394187881

Gene: CLCN7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1450668T>C , CM000678.2:g.1450668T>C	GRCh38
NC_000016.9:g.1500669T>C , CM000678.1:g.1500669T>C	GRCh37
NC_000016.8:g.1440670T>C	NCBI36
NG_007567.1:g.29417A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001287.6:c.1448-2A>G MANE Select	NP_001278.1:n.1448-2A>G
ENST00000382745.9:c.1448-2A>G MANE Select	ENSP00000372193.4:n.1448-2A>G
NM_001114331.2:c.1376-2A>G	NP_001107803.1:n.1376-2A>G
NM_001114331.3:c.1376-2A>G	NP_001107803.1:n.1376-2A>G
NM_001287.5:c.1448-2A>G	NP_001278.1:n.1448-2A>G
ENST00000262318.12:c.1376-2A>G	ENSP00000262318.8:n.1376-2A>G
ENST00000382745.8:c.1448-2A>G	ENSP00000372193.4:n.1448-2A>G
ENST00000448525.5:c.1376-2A>G	ENSP00000410907.1:n.1376-2A>G
ENST00000563642.6:n.348-2A>G
ENST00000699947.1:c.1448-2A>G	ENSP00000514703.1:n.1448-2A>G
ENST00000699948.1:c.1454-2A>G	ENSP00000514704.1:n.1454-2A>G
XM_011522354.1:c.1274-2A>G	XP_011520656.1:n.1274-2A>G