Canonical Allele Identifier: CA1748897688

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143350511A= , CM000669.2:g.143350511A=	GRCh38
NC_000007.13:g.143047604A= , CM000669.1:g.143047604A=	GRCh37
NC_000007.12:g.142757726A=	NCBI36
NG_009815.1:g.39386A=
NG_009815.2:g.39386A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2508+35A=	ENSP00000498052.2:n.2508+35A=
ENST00000343257.7:c.2508+35A= MANE Select	ENSP00000339867.2:n.2508+35A=
ENST00000432192.6:c.2332+35A=
ENST00000343257.6:c.2508+35A=	ENSP00000339867.2:n.2508+35A=
NM_000083.2:c.2508+35A=	NP_000074.2:n.2508+35A=
NR_046453.1:n.2448+35A=
XM_011515781.1:c.2532+35A=	XP_011514083.1:n.2532+35A=
XM_011515782.1:c.1254+35A=	XP_011514084.1:n.1254+35A=
XM_011515782.2:c.1254+35A=	XP_011514084.1:n.1254+35A=
XM_017011739.1:c.2082+35A=	XP_016867228.1:n.2082+35A=
XM_017011740.1:c.2058+35A=	XP_016867229.1:n.2058+35A=
NM_000083.3:c.2508+35A= MANE Select	NP_000074.3:n.2508+35A=
NR_046453.2:n.2463+35A=