Canonical Allele Identifier: CA1748889059

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143331107T= , CM000669.2:g.143331107T=	GRCh38
NC_000007.13:g.143028200T= , CM000669.1:g.143028200T=	GRCh37
NC_000007.12:g.142738322T=	NCBI36
NG_009815.1:g.19982T=
NG_009815.2:g.19982T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.980-125T=	ENSP00000498052.2:n.980-125T=
ENST00000343257.7:c.980-125T= MANE Select	ENSP00000339867.2:n.980-125T=
ENST00000432192.6:c.804-125T=
ENST00000343257.6:c.980-125T=	ENSP00000339867.2:n.980-125T=
NM_000083.2:c.980-125T=	NP_000074.2:n.980-125T=
NR_046453.1:n.1070-125T=
XM_011515781.1:c.980-125T=	XP_011514083.1:n.980-125T=
XM_017011739.1:c.530-125T=	XP_016867228.1:n.530-125T=
XM_017011740.1:c.530-125T=	XP_016867229.1:n.530-125T=
NM_000083.3:c.980-125T= MANE Select	NP_000074.3:n.980-125T=
NR_046453.2:n.1085-125T=