Canonical Allele Identifier: CA1748892759

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339267C= , CM000669.2:g.143339267C=	GRCh38
NC_000007.13:g.143036360C= , CM000669.1:g.143036360C=	GRCh37
NC_000007.12:g.142746482C=	NCBI36
NG_009815.1:g.28142C=
NG_009815.2:g.28142C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1416C=	ENSP00000498052.2:p.Ile472=
ENST00000343257.7:c.1416C= MANE Select	ENSP00000339867.2:p.Ile472=
ENST00000432192.6:c.1240C=
ENST00000343257.6:c.1416C=	ENSP00000339867.2:p.Ile472=
NM_000083.2:c.1416C=	NP_000074.2:p.Ile472=
NR_046453.1:n.1356C=
XM_011515781.1:c.1440C=	XP_011514083.1:p.Ile480=
XM_011515782.1:c.162C=	XP_011514084.1:p.Ile54=
XM_011515782.2:c.162C=	XP_011514084.1:p.Ile54=
XM_017011739.1:c.990C=	XP_016867228.1:p.Ile330=
XM_017011740.1:c.966C=	XP_016867229.1:p.Ile322=
NM_000083.3:c.1416C= MANE Select	NP_000074.3:p.Ile472=
NR_046453.2:n.1371C=