Canonical Allele Identifier: CA2428768780

Gene: CLCN5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50086149A= , CM000685.2:g.50086149A=	GRCh38
NC_000023.10:g.49850806A= , CM000685.1:g.49850806A=	GRCh37
NC_000023.9:g.49737546A=	NCBI36
NG_007159.3:g.168534A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376091.8:c.1014+89A= MANE Select	ENSP00000365259.3:n.1014+89A=
ENST00000642383.1:c.264+89A=	ENSP00000496353.1:n.264+89A=
ENST00000642885.1:c.804+89A=	ENSP00000496632.1:n.804+89A=
ENST00000643129.1:c.1301+89A=
ENST00000646398.1:c.*189+89A=	ENSP00000495122.1:n.*189+89A=
ENST00000307367.2:c.804+89A=	ENSP00000304257.2:n.804+89A=
ENST00000376088.7:c.1014+89A=	ENSP00000365256.3:n.1014+89A=
ENST00000376091.7:c.1014+89A=	ENSP00000365259.3:n.1014+89A=
ENST00000376108.7:c.804+89A=	ENSP00000365276.3:n.804+89A=
NM_000084.4:c.804+89A=	NP_000075.1:n.804+89A=
NM_001127898.3:c.1014+89A=	NP_001121370.1:n.1014+89A=
NM_001127899.3:c.1014+89A=	NP_001121371.1:n.1014+89A=
NM_001282163.1:c.864+89A=	NP_001269092.1:n.864+89A=
XM_011543888.1:c.1014+89A=	XP_011542190.1:n.1014+89A=
XM_011543889.1:c.804+89A=	XP_011542191.1:n.804+89A=
XM_017029257.1:c.1026+89A=	XP_016884746.1:n.1026+89A=
XM_017029258.1:c.1026+89A=	XP_016884747.1:n.1026+89A=
NM_001127898.4:c.1014+89A= MANE Select	NP_001121370.1:n.1014+89A=
NM_000084.5:c.804+89A=	NP_000075.1:n.804+89A=
NM_001127899.4:c.1014+89A=	NP_001121371.1:n.1014+89A=
NM_001282163.2:c.864+89A=	NP_001269092.1:n.864+89A=