Canonical Allele Identifier: CA516678512

Gene: CLCN5

Linked Data

• MyVariant Identifiers: chrX:g.49851215G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50086558G>C , CM000685.2:g.50086558G>C	GRCh38
NC_000023.10:g.49851215G>C , CM000685.1:g.49851215G>C	GRCh37
NC_000023.9:g.49737955G>C	NCBI36
NG_007159.3:g.168943G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376091.8:c.1245G>C MANE Select	ENSP00000365259.3:p.Arg415=
ENST00000642383.1:c.495G>C	ENSP00000496353.1:p.Arg165=
ENST00000642885.1:c.1035G>C	ENSP00000496632.1:p.Arg345=
ENST00000643129.1:c.1532G>C
ENST00000646398.1:c.*420G>C	ENSP00000495122.1:n.*420G>C
ENST00000307367.2:c.1035G>C	ENSP00000304257.2:p.Arg345=
ENST00000376088.7:c.1245G>C	ENSP00000365256.3:p.Arg415=
ENST00000376091.7:c.1245G>C	ENSP00000365259.3:p.Arg415=
ENST00000376108.7:c.1035G>C	ENSP00000365276.3:p.Arg345=
NM_000084.4:c.1035G>C	NP_000075.1:p.Arg345=
NM_001127898.3:c.1245G>C	NP_001121370.1:p.Arg415=
NM_001127899.3:c.1245G>C	NP_001121371.1:p.Arg415=
NM_001282163.1:c.1095G>C	NP_001269092.1:p.Arg365=
XM_011543888.1:c.1245G>C	XP_011542190.1:p.Arg415=
XM_011543889.1:c.1035G>C	XP_011542191.1:p.Arg345=
XM_017029257.1:c.1257G>C	XP_016884746.1:p.Arg419=
XM_017029258.1:c.1257G>C	XP_016884747.1:p.Arg419=
NM_001127898.4:c.1245G>C MANE Select	NP_001121370.1:p.Arg415=
NM_000084.5:c.1035G>C	NP_000075.1:p.Arg345=
NM_001127899.4:c.1245G>C	NP_001121371.1:p.Arg415=
NM_001282163.2:c.1095G>C	NP_001269092.1:p.Arg365=