Canonical Allele Identifier: CA1748889082

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143331163G= , CM000669.2:g.143331163G=	GRCh38
NC_000007.13:g.143028256G= , CM000669.1:g.143028256G=	GRCh37
NC_000007.12:g.142738378G=	NCBI36
NG_009815.1:g.20038G=
NG_009815.2:g.20038G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.980-69G=	ENSP00000498052.2:n.980-69G=
ENST00000343257.7:c.980-69G= MANE Select	ENSP00000339867.2:n.980-69G=
ENST00000432192.6:c.804-69G=
ENST00000343257.6:c.980-69G=	ENSP00000339867.2:n.980-69G=
NM_000083.2:c.980-69G=	NP_000074.2:n.980-69G=
NR_046453.1:n.1070-69G=
XM_011515781.1:c.980-69G=	XP_011514083.1:n.980-69G=
XM_017011739.1:c.530-69G=	XP_016867228.1:n.530-69G=
XM_017011740.1:c.530-69G=	XP_016867229.1:n.530-69G=
NM_000083.3:c.980-69G= MANE Select	NP_000074.3:n.980-69G=
NR_046453.2:n.1085-69G=