Canonical Allele Identifier: CA516678328

Gene: CLCN5

Linked Data

• MyVariant Identifiers: chrX:g.49851302T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50086645T>C , CM000685.2:g.50086645T>C	GRCh38
NC_000023.10:g.49851302T>C , CM000685.1:g.49851302T>C	GRCh37
NC_000023.9:g.49738042T>C	NCBI36
NG_007159.3:g.169030T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376091.8:c.1332T>C MANE Select	ENSP00000365259.3:p.Asn444=
ENST00000642383.1:c.582T>C	ENSP00000496353.1:p.Asn194=
ENST00000642885.1:c.1122T>C	ENSP00000496632.1:p.Asn374=
ENST00000643129.1:c.1619T>C
ENST00000646398.1:c.*507T>C	ENSP00000495122.1:n.*507T>C
ENST00000307367.2:c.1122T>C	ENSP00000304257.2:p.Asn374=
ENST00000376088.7:c.1332T>C	ENSP00000365256.3:p.Asn444=
ENST00000376091.7:c.1332T>C	ENSP00000365259.3:p.Asn444=
ENST00000376108.7:c.1122T>C	ENSP00000365276.3:p.Asn374=
NM_000084.4:c.1122T>C	NP_000075.1:p.Asn374=
NM_001127898.3:c.1332T>C	NP_001121370.1:p.Asn444=
NM_001127899.3:c.1332T>C	NP_001121371.1:p.Asn444=
NM_001282163.1:c.1182T>C	NP_001269092.1:p.Asn394=
XM_011543888.1:c.1332T>C	XP_011542190.1:p.Asn444=
XM_011543889.1:c.1122T>C	XP_011542191.1:p.Asn374=
XM_017029257.1:c.1344T>C	XP_016884746.1:p.Asn448=
XM_017029258.1:c.1344T>C	XP_016884747.1:p.Asn448=
NM_001127898.4:c.1332T>C MANE Select	NP_001121370.1:p.Asn444=
NM_000084.5:c.1122T>C	NP_000075.1:p.Asn374=
NM_001127899.4:c.1332T>C	NP_001121371.1:p.Asn444=
NM_001282163.2:c.1182T>C	NP_001269092.1:p.Asn394=