Canonical Allele Identifier: CA1748888925

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330847C= , CM000669.2:g.143330847C=	GRCh38
NC_000007.13:g.143027940C= , CM000669.1:g.143027940C=	GRCh37
NC_000007.12:g.142738062C=	NCBI36
NG_009815.1:g.19722C=
NG_009815.2:g.19722C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.929C=	ENSP00000498052.2:p.Thr310=
ENST00000343257.7:c.929C= MANE Select	ENSP00000339867.2:p.Thr310=
ENST00000432192.6:c.753C=
ENST00000455478.6:c.517C=	ENSP00000400027.2:n.517C=
ENST00000650516.1:c.929C=	ENSP00000498052.1:p.Thr310=
ENST00000343257.6:c.929C=	ENSP00000339867.2:p.Thr310=
ENST00000432192.5:c.443C=
ENST00000455478.5:c.521C=
ENST00000495612.1:n.230C=
NM_000083.2:c.929C=	NP_000074.2:p.Thr310=
NR_046453.1:n.1019C=
XM_011515781.1:c.929C=	XP_011514083.1:p.Thr310=
XM_017011739.1:c.479C=	XP_016867228.1:p.Thr160=
XM_017011740.1:c.479C=	XP_016867229.1:p.Thr160=
NM_000083.3:c.929C= MANE Select	NP_000074.3:p.Thr310=
NR_046453.2:n.1034C=