Canonical Allele Identifier: CA1748888119

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321408G= , CM000669.2:g.143321408G=	GRCh38
NC_000007.13:g.143018501G= , CM000669.1:g.143018501G=	GRCh37
NC_000007.12:g.142728623G=	NCBI36
NG_009815.1:g.10283G=
NG_009815.2:g.10283G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.477G=	ENSP00000498052.2:p.Leu159=
ENST00000343257.7:c.477G= MANE Select	ENSP00000339867.2:p.Leu159=
ENST00000432192.6:c.245G=
ENST00000650516.1:c.477G=	ENSP00000498052.1:p.Leu159=
ENST00000343257.6:c.477G=	ENSP00000339867.2:p.Leu159=
NM_000083.2:c.477G=	NP_000074.2:p.Leu159=
NR_046453.1:n.564G=
XM_011515781.1:c.477G=	XP_011514083.1:p.Leu159=
XM_017011739.1:c.184G=	XP_016867228.1:p.Ala62=
XM_017011740.1:c.184G=	XP_016867229.1:p.Ala62=
NM_000083.3:c.477G= MANE Select	NP_000074.3:p.Leu159=
NR_046453.2:n.579G=