Canonical Allele Identifier: CA2428768880

Gene: CLCN5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50086480C= , CM000685.2:g.50086480C=	GRCh38
NC_000023.10:g.49851137C= , CM000685.1:g.49851137C=	GRCh37
NC_000023.9:g.49737877C=	NCBI36
NG_007159.3:g.168865C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376091.8:c.1167C= MANE Select	ENSP00000365259.3:p.Leu389=
ENST00000642383.1:c.417C=	ENSP00000496353.1:p.Leu139=
ENST00000642885.1:c.957C=	ENSP00000496632.1:p.Leu319=
ENST00000643129.1:c.1454C=
ENST00000646398.1:c.*342C=	ENSP00000495122.1:n.*342C=
ENST00000307367.2:c.957C=	ENSP00000304257.2:p.Leu319=
ENST00000376088.7:c.1167C=	ENSP00000365256.3:p.Leu389=
ENST00000376091.7:c.1167C=	ENSP00000365259.3:p.Leu389=
ENST00000376108.7:c.957C=	ENSP00000365276.3:p.Leu319=
NM_000084.4:c.957C=	NP_000075.1:p.Leu319=
NM_001127898.3:c.1167C=	NP_001121370.1:p.Leu389=
NM_001127899.3:c.1167C=	NP_001121371.1:p.Leu389=
NM_001282163.1:c.1017C=	NP_001269092.1:p.Leu339=
XM_011543888.1:c.1167C=	XP_011542190.1:p.Leu389=
XM_011543889.1:c.957C=	XP_011542191.1:p.Leu319=
XM_017029257.1:c.1179C=	XP_016884746.1:p.Leu393=
XM_017029258.1:c.1179C=	XP_016884747.1:p.Leu393=
NM_001127898.4:c.1167C= MANE Select	NP_001121370.1:p.Leu389=
NM_000084.5:c.957C=	NP_000075.1:p.Leu319=
NM_001127899.4:c.1167C=	NP_001121371.1:p.Leu389=
NM_001282163.2:c.1017C=	NP_001269092.1:p.Leu339=