Canonical Allele Identifier: CA10413861

Gene: CLCN5

Linked Data

• ClinVar Variation Id: 1138734
• ClinVar RCV Id: RCV001475213
• dbSNP Id: rs782265386
• ExAC: X:49851272 A / G
• gnomAD v2: X-49851272-A-G
• gnomAD v3: X-50086615-A-G
• gnomAD v4: X-50086615-A-G
• MyVariant Identifiers: chrX:g.49851272A>G (hg19) ; chrX:g.50086615A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50086615A>G , CM000685.2:g.50086615A>G	GRCh38
NC_000023.10:g.49851272A>G , CM000685.1:g.49851272A>G	GRCh37
NC_000023.9:g.49738012A>G	NCBI36
NG_007159.3:g.169000A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376091.8:c.1302A>G MANE Select	ENSP00000365259.3:p.Thr434=
ENST00000642383.1:c.552A>G	ENSP00000496353.1:p.Thr184=
ENST00000642885.1:c.1092A>G	ENSP00000496632.1:p.Thr364=
ENST00000643129.1:c.1589A>G
ENST00000646398.1:c.*477A>G	ENSP00000495122.1:n.*477A>G
ENST00000307367.2:c.1092A>G	ENSP00000304257.2:p.Thr364=
ENST00000376088.7:c.1302A>G	ENSP00000365256.3:p.Thr434=
ENST00000376091.7:c.1302A>G	ENSP00000365259.3:p.Thr434=
ENST00000376108.7:c.1092A>G	ENSP00000365276.3:p.Thr364=
NM_000084.4:c.1092A>G	NP_000075.1:p.Thr364=
NM_001127898.3:c.1302A>G	NP_001121370.1:p.Thr434=
NM_001127899.3:c.1302A>G	NP_001121371.1:p.Thr434=
NM_001282163.1:c.1152A>G	NP_001269092.1:p.Thr384=
XM_011543888.1:c.1302A>G	XP_011542190.1:p.Thr434=
XM_011543889.1:c.1092A>G	XP_011542191.1:p.Thr364=
XM_017029257.1:c.1314A>G	XP_016884746.1:p.Thr438=
XM_017029258.1:c.1314A>G	XP_016884747.1:p.Thr438=
NM_001127898.4:c.1302A>G MANE Select	NP_001121370.1:p.Thr434=
NM_000084.5:c.1092A>G	NP_000075.1:p.Thr364=
NM_001127899.4:c.1302A>G	NP_001121371.1:p.Thr434=
NM_001282163.2:c.1152A>G	NP_001269092.1:p.Thr384=