Canonical Allele Identifier: CA2428768908

Gene: CLCN5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50086570C= , CM000685.2:g.50086570C=	GRCh38
NC_000023.10:g.49851227C= , CM000685.1:g.49851227C=	GRCh37
NC_000023.9:g.49737967C=	NCBI36
NG_007159.3:g.168955C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376091.8:c.1257C= MANE Select	ENSP00000365259.3:p.Thr419=
ENST00000642383.1:c.507C=	ENSP00000496353.1:p.Thr169=
ENST00000642885.1:c.1047C=	ENSP00000496632.1:p.Thr349=
ENST00000643129.1:c.1544C=
ENST00000646398.1:c.*432C=	ENSP00000495122.1:n.*432C=
ENST00000307367.2:c.1047C=	ENSP00000304257.2:p.Thr349=
ENST00000376088.7:c.1257C=	ENSP00000365256.3:p.Thr419=
ENST00000376091.7:c.1257C=	ENSP00000365259.3:p.Thr419=
ENST00000376108.7:c.1047C=	ENSP00000365276.3:p.Thr349=
NM_000084.4:c.1047C=	NP_000075.1:p.Thr349=
NM_001127898.3:c.1257C=	NP_001121370.1:p.Thr419=
NM_001127899.3:c.1257C=	NP_001121371.1:p.Thr419=
NM_001282163.1:c.1107C=	NP_001269092.1:p.Thr369=
XM_011543888.1:c.1257C=	XP_011542190.1:p.Thr419=
XM_011543889.1:c.1047C=	XP_011542191.1:p.Thr349=
XM_017029257.1:c.1269C=	XP_016884746.1:p.Thr423=
XM_017029258.1:c.1269C=	XP_016884747.1:p.Thr423=
NM_001127898.4:c.1257C= MANE Select	NP_001121370.1:p.Thr419=
NM_000084.5:c.1047C=	NP_000075.1:p.Thr349=
NM_001127899.4:c.1257C=	NP_001121371.1:p.Thr419=
NM_001282163.2:c.1107C=	NP_001269092.1:p.Thr369=