Canonical Allele Identifier: CA1748893926

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143341987C= , CM000669.2:g.143341987C=	GRCh38
NC_000007.13:g.143039080C= , CM000669.1:g.143039080C=	GRCh37
NC_000007.12:g.142749202C=	NCBI36
NG_009815.1:g.30862C=
NG_009815.2:g.30862C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1641C=	ENSP00000498052.2:p.Phe547=
ENST00000343257.7:c.1641C= MANE Select	ENSP00000339867.2:p.Phe547=
ENST00000432192.6:c.1465C=
ENST00000343257.6:c.1641C=	ENSP00000339867.2:p.Phe547=
NM_000083.2:c.1641C=	NP_000074.2:p.Phe547=
NR_046453.1:n.1581C=
XM_011515781.1:c.1665C=	XP_011514083.1:p.Phe555=
XM_011515782.1:c.387C=	XP_011514084.1:p.Phe129=
XM_011515782.2:c.387C=	XP_011514084.1:p.Phe129=
XM_017011739.1:c.1215C=	XP_016867228.1:p.Phe405=
XM_017011740.1:c.1191C=	XP_016867229.1:p.Phe397=
NM_000083.3:c.1641C= MANE Select	NP_000074.3:p.Phe547=
NR_046453.2:n.1596C=