Canonical Allele Identifier: CA1748882070

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143322024A= , CM000669.2:g.143322024A=	GRCh38
NC_000007.13:g.143019117A= , CM000669.1:g.143019117A=	GRCh37
NC_000007.12:g.142729239A=	NCBI36
NG_009815.1:g.10899A=
NG_009815.2:g.10899A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.696+176A=	ENSP00000498052.2:n.696+176A=
ENST00000343257.7:c.696+176A= MANE Select	ENSP00000339867.2:n.696+176A=
ENST00000432192.6:c.464+176A=
ENST00000455478.6:c.150+176A=	ENSP00000400027.2:n.150+176A=
ENST00000650516.1:c.696+176A=	ENSP00000498052.1:n.696+176A=
ENST00000343257.6:c.696+176A=	ENSP00000339867.2:n.696+176A=
ENST00000432192.5:c.154+176A=
ENST00000455478.5:c.154+176A=
ENST00000495612.1:n.154+176A=
NM_000083.2:c.696+176A=	NP_000074.2:n.696+176A=
NR_046453.1:n.783+176A=
XM_011515781.1:c.696+176A=	XP_011514083.1:n.696+176A=
XM_017011739.1:c.403+176A=	XP_016867228.1:n.403+176A=
XM_017011740.1:c.403+176A=	XP_016867229.1:n.403+176A=
NM_000083.3:c.696+176A= MANE Select	NP_000074.3:n.696+176A=
NR_046453.2:n.798+176A=