Canonical Allele Identifier: CA413185585

Gene: CLCN5

Linked Data

• dbSNP Id: rs1557193976
• gnomAD v2: X-49851253-T-C
• gnomAD v4: X-50086596-T-C
• MyVariant Identifiers: chrX:g.49851253T>C (hg19) ; chrX:g.50086596T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50086596T>C , CM000685.2:g.50086596T>C	GRCh38
NC_000023.10:g.49851253T>C , CM000685.1:g.49851253T>C	GRCh37
NC_000023.9:g.49737993T>C	NCBI36
NG_007159.3:g.168981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376091.8:c.1283T>C MANE Select	ENSP00000365259.3:p.Ile428Thr
ENST00000642383.1:c.533T>C	ENSP00000496353.1:p.Ile178Thr
ENST00000642885.1:c.1073T>C	ENSP00000496632.1:p.Ile358Thr
ENST00000643129.1:c.1570T>C
ENST00000646398.1:c.*458T>C	ENSP00000495122.1:n.*458T>C
ENST00000307367.2:c.1073T>C	ENSP00000304257.2:p.Ile358Thr
ENST00000376088.7:c.1283T>C	ENSP00000365256.3:p.Ile428Thr
ENST00000376091.7:c.1283T>C	ENSP00000365259.3:p.Ile428Thr
ENST00000376108.7:c.1073T>C	ENSP00000365276.3:p.Ile358Thr
NM_000084.4:c.1073T>C	NP_000075.1:p.Ile358Thr
NM_001127898.3:c.1283T>C	NP_001121370.1:p.Ile428Thr
NM_001127899.3:c.1283T>C	NP_001121371.1:p.Ile428Thr
NM_001282163.1:c.1133T>C	NP_001269092.1:p.Ile378Thr
XM_011543888.1:c.1283T>C	XP_011542190.1:p.Ile428Thr
XM_011543889.1:c.1073T>C	XP_011542191.1:p.Ile358Thr
XM_017029257.1:c.1295T>C	XP_016884746.1:p.Ile432Thr
XM_017029258.1:c.1295T>C	XP_016884747.1:p.Ile432Thr
NM_001127898.4:c.1283T>C MANE Select	NP_001121370.1:p.Ile428Thr
NM_000084.5:c.1073T>C	NP_000075.1:p.Ile358Thr
NM_001127899.4:c.1283T>C	NP_001121371.1:p.Ile428Thr
NM_001282163.2:c.1133T>C	NP_001269092.1:p.Ile378Thr