Canonical Allele Identifier: CA10413717

Gene: CLCN5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50072515A>G , CM000685.2:g.50072515A>G	GRCh38
NC_000023.10:g.49837170A>G , CM000685.1:g.49837170A>G	GRCh37
NC_000023.9:g.49723910A>G	NCBI36
NG_007159.3:g.154900A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001127898.4:c.342A>G MANE Select	NP_001121370.1:p.Thr114=
ENST00000376091.8:c.342A>G MANE Select	ENSP00000365259.3:p.Thr114=
NM_000084.4:c.132A>G	NP_000075.1:p.Thr44=
NM_000084.5:c.132A>G	NP_000075.1:p.Thr44=
NM_001127898.3:c.342A>G	NP_001121370.1:p.Thr114=
NM_001127899.3:c.342A>G	NP_001121371.1:p.Thr114=
NM_001127899.4:c.342A>G	NP_001121371.1:p.Thr114=
NM_001282163.1:c.192A>G	NP_001269092.1:p.Thr64=
NM_001282163.2:c.192A>G	NP_001269092.1:p.Thr64=
ENST00000307367.2:c.132A>G	ENSP00000304257.2:p.Thr44=
ENST00000376088.7:c.342A>G	ENSP00000365256.3:p.Thr114=
ENST00000376091.7:c.342A>G	ENSP00000365259.3:p.Thr114=
ENST00000376108.7:c.132A>G	ENSP00000365276.3:p.Thr44=
ENST00000642885.1:c.132A>G	ENSP00000496632.1:p.Thr44=
ENST00000643129.1:c.629A>G
ENST00000646398.1:c.132A>G	ENSP00000495122.1:p.Thr44=
XM_011543888.1:c.342A>G	XP_011542190.1:p.Thr114=
XM_011543889.1:c.132A>G	XP_011542191.1:p.Thr44=
XM_017029257.1:c.354A>G	XP_016884746.1:p.Thr118=
XM_017029258.1:c.354A>G	XP_016884747.1:p.Thr118=