Canonical Allele Identifier: CA1748887331

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143320756A= , CM000669.2:g.143320756A=	GRCh38
NC_000007.13:g.143017849A= , CM000669.1:g.143017849A=	GRCh37
NC_000007.12:g.142727971A=	NCBI36
NG_009815.1:g.9631A=
NG_009815.2:g.9631A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.394A=	ENSP00000498052.2:p.Ser132=
ENST00000343257.7:c.394A= MANE Select	ENSP00000339867.2:p.Ser132=
ENST00000432192.6:c.162A=
ENST00000650516.1:c.394A=	ENSP00000498052.1:p.Ser132=
ENST00000343257.6:c.394A=	ENSP00000339867.2:p.Ser132=
NM_000083.2:c.394A=	NP_000074.2:p.Ser132=
NR_046453.1:n.481A=
XM_011515781.1:c.394A=	XP_011514083.1:p.Ser132=
XM_017011739.1:c.101A=	XP_016867228.1:p.Gln34=
XM_017011740.1:c.101A=	XP_016867229.1:p.Gln34=
NM_000083.3:c.394A= MANE Select	NP_000074.3:p.Ser132=
NR_046453.2:n.496A=