Canonical Allele Identifier: CA413185116

Gene: CLCN5

Linked Data

• MyVariant Identifiers: chrX:g.49851034C>T (hg19) ; chrX:g.50086377C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50086377C>T , CM000685.2:g.50086377C>T	GRCh38
NC_000023.10:g.49851034C>T , CM000685.1:g.49851034C>T	GRCh37
NC_000023.9:g.49737774C>T	NCBI36
NG_007159.3:g.168762C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376091.8:c.1064C>T MANE Select	ENSP00000365259.3:p.Ala355Val
ENST00000642383.1:c.314C>T	ENSP00000496353.1:p.Ala105Val
ENST00000642885.1:c.854C>T	ENSP00000496632.1:p.Ala285Val
ENST00000643129.1:c.1351C>T
ENST00000646398.1:c.*239C>T	ENSP00000495122.1:n.*239C>T
ENST00000307367.2:c.854C>T	ENSP00000304257.2:p.Ala285Val
ENST00000376088.7:c.1064C>T	ENSP00000365256.3:p.Ala355Val
ENST00000376091.7:c.1064C>T	ENSP00000365259.3:p.Ala355Val
ENST00000376108.7:c.854C>T	ENSP00000365276.3:p.Ala285Val
NM_000084.4:c.854C>T	NP_000075.1:p.Ala285Val
NM_001127898.3:c.1064C>T	NP_001121370.1:p.Ala355Val
NM_001127899.3:c.1064C>T	NP_001121371.1:p.Ala355Val
NM_001282163.1:c.914C>T	NP_001269092.1:p.Ala305Val
XM_011543888.1:c.1064C>T	XP_011542190.1:p.Ala355Val
XM_011543889.1:c.854C>T	XP_011542191.1:p.Ala285Val
XM_017029257.1:c.1076C>T	XP_016884746.1:p.Ala359Val
XM_017029258.1:c.1076C>T	XP_016884747.1:p.Ala359Val
NM_001127898.4:c.1064C>T MANE Select	NP_001121370.1:p.Ala355Val
NM_000084.5:c.854C>T	NP_000075.1:p.Ala285Val
NM_001127899.4:c.1064C>T	NP_001121371.1:p.Ala355Val
NM_001282163.2:c.914C>T	NP_001269092.1:p.Ala305Val