Canonical Allele Identifier: CA1748888158

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321427A= , CM000669.2:g.143321427A=	GRCh38
NC_000007.13:g.143018520A= , CM000669.1:g.143018520A=	GRCh37
NC_000007.12:g.142728642A=	NCBI36
NG_009815.1:g.10302A=
NG_009815.2:g.10302A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.496A=	ENSP00000498052.2:p.Thr166=
ENST00000343257.7:c.496A= MANE Select	ENSP00000339867.2:p.Thr166=
ENST00000432192.6:c.264A=
ENST00000650516.1:c.496A=	ENSP00000498052.1:p.Thr166=
ENST00000343257.6:c.496A=	ENSP00000339867.2:p.Thr166=
NM_000083.2:c.496A=	NP_000074.2:p.Thr166=
NR_046453.1:n.583A=
XM_011515781.1:c.496A=	XP_011514083.1:p.Thr166=
XM_017011739.1:c.203A=	XP_016867228.1:p.His68=
XM_017011740.1:c.203A=	XP_016867229.1:p.His68=
NM_000083.3:c.496A= MANE Select	NP_000074.3:p.Thr166=
NR_046453.2:n.598A=