Canonical Allele Identifier: CA2805555460

Gene: CLCN7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1447169_1447171dup , CM000678.2:g.1447169_1447171dup	GRCh38
NC_000016.9:g.1497170_1497172dup , CM000678.1:g.1497170_1497172dup	GRCh37
NC_000016.8:g.1437171_1437173dup	NCBI36
NG_007567.1:g.32917_32919dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699947.1:c.2251-82_2251-80dup	ENSP00000514703.1:n.2251-82_2251-80dup
ENST00000699948.1:c.*564-82_*564-80dup	ENSP00000514704.1:n.*564-82_*564-80dup
ENST00000382745.9:c.2251-82_2251-80dup MANE Select	ENSP00000372193.4:n.2251-82_2251-80dup
ENST00000262318.12:c.2183-85_2183-83dup	ENSP00000262318.8:n.2183-85_2183-83dup
ENST00000382745.8:c.2251-82_2251-80dup	ENSP00000372193.4:n.2251-82_2251-80dup
ENST00000448525.5:c.2179-82_2179-80dup	ENSP00000410907.1:n.2179-82_2179-80dup
ENST00000563642.6:n.2320-82_2320-80dup
ENST00000565092.6:n.1286-82_1286-80dup
ENST00000567836.2:n.492-82_492-80dup
NM_001114331.2:c.2179-82_2179-80dup	NP_001107803.1:n.2179-82_2179-80dup
NM_001287.5:c.2251-82_2251-80dup	NP_001278.1:n.2251-82_2251-80dup
XM_011522354.1:c.2077-82_2077-80dup	XP_011520656.1:n.2077-82_2077-80dup
NM_001287.6:c.2251-82_2251-80dup MANE Select	NP_001278.1:n.2251-82_2251-80dup
NM_001114331.3:c.2179-82_2179-80dup	NP_001107803.1:n.2179-82_2179-80dup