Canonical Allele Identifier: CA1748898272

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351664A= , CM000669.2:g.143351664A=	GRCh38
NC_000007.13:g.143048757A= , CM000669.1:g.143048757A=	GRCh37
NC_000007.12:g.142758879A=	NCBI36
NG_009815.1:g.40539A=
NG_009815.2:g.40539A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2666A=	ENSP00000498052.2:p.Asn889=
ENST00000343257.7:c.2666A= MANE Select	ENSP00000339867.2:p.Asn889=
ENST00000432192.6:c.2490A=
ENST00000343257.6:c.2666A=	ENSP00000339867.2:p.Asn889=
NM_000083.2:c.2666A=	NP_000074.2:p.Asn889=
NR_046453.1:n.2606A=
XM_011515781.1:c.2690A=	XP_011514083.1:p.Asn897=
XM_011515782.1:c.1412A=	XP_011514084.1:p.Asn471=
XM_011515782.2:c.1412A=	XP_011514084.1:p.Asn471=
XM_017011739.1:c.2240A=	XP_016867228.1:p.Asn747=
XM_017011740.1:c.2216A=	XP_016867229.1:p.Asn739=
NM_000083.3:c.2666A= MANE Select	NP_000074.3:p.Asn889=
NR_046453.2:n.2621A=