Canonical Allele Identifier: CA1748898271

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351661G= , CM000669.2:g.143351661G=	GRCh38
NC_000007.13:g.143048754G= , CM000669.1:g.143048754G=	GRCh37
NC_000007.12:g.142758876G=	NCBI36
NG_009815.1:g.40536G=
NG_009815.2:g.40536G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2663G=	ENSP00000498052.2:p.Arg888=
ENST00000343257.7:c.2663G= MANE Select	ENSP00000339867.2:p.Arg888=
ENST00000432192.6:c.2487G=
ENST00000343257.6:c.2663G=	ENSP00000339867.2:p.Arg888=
NM_000083.2:c.2663G=	NP_000074.2:p.Arg888=
NR_046453.1:n.2603G=
XM_011515781.1:c.2687G=	XP_011514083.1:p.Arg896=
XM_011515782.1:c.1409G=	XP_011514084.1:p.Arg470=
XM_011515782.2:c.1409G=	XP_011514084.1:p.Arg470=
XM_017011739.1:c.2237G=	XP_016867228.1:p.Arg746=
XM_017011740.1:c.2213G=	XP_016867229.1:p.Arg738=
NM_000083.3:c.2663G= MANE Select	NP_000074.3:p.Arg888=
NR_046453.2:n.2618G=