Canonical Allele Identifier: CA2630989947

Gene: CLCN7

Linked Data

• gnomAD v4: 16-1447120-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447120A>G , CM000678.2:g.1447120A>G	GRCh38
NC_000016.9:g.1497121A>G , CM000678.1:g.1497121A>G	GRCh37
NC_000016.8:g.1437122A>G	NCBI36
NG_007567.1:g.32965T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2251-34T>C	ENSP00000514703.1:n.2251-34T>C
ENST00000699948.1:c.*564-34T>C	ENSP00000514704.1:n.*564-34T>C
ENST00000382745.9:c.2251-34T>C MANE Select	ENSP00000372193.4:n.2251-34T>C
ENST00000262318.12:c.2183-37T>C	ENSP00000262318.8:n.2183-37T>C
ENST00000382745.8:c.2251-34T>C	ENSP00000372193.4:n.2251-34T>C
ENST00000448525.5:c.2179-34T>C	ENSP00000410907.1:n.2179-34T>C
ENST00000563642.6:n.2320-34T>C
ENST00000565092.6:n.1286-34T>C
ENST00000567836.2:n.492-34T>C
NM_001114331.2:c.2179-34T>C	NP_001107803.1:n.2179-34T>C
NM_001287.5:c.2251-34T>C	NP_001278.1:n.2251-34T>C
XM_011522354.1:c.2077-34T>C	XP_011520656.1:n.2077-34T>C
NM_001287.6:c.2251-34T>C MANE Select	NP_001278.1:n.2251-34T>C
NM_001114331.3:c.2179-34T>C	NP_001107803.1:n.2179-34T>C