Canonical Allele Identifier: CA1748889650

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332499G= , CM000669.2:g.143332499G=	GRCh38
NC_000007.13:g.143029592G= , CM000669.1:g.143029592G=	GRCh37
NC_000007.12:g.142739714G=	NCBI36
NG_009815.1:g.21374G=
NG_009815.2:g.21374G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1247G=	ENSP00000498052.2:p.Gly416=
ENST00000343257.7:c.1247G= MANE Select	ENSP00000339867.2:p.Gly416=
ENST00000432192.6:c.1071G=
ENST00000343257.6:c.1247G=	ENSP00000339867.2:p.Gly416=
NM_000083.2:c.1247G=	NP_000074.2:p.Gly416=
NR_046453.1:n.1337G=
XM_011515781.1:c.1247G=	XP_011514083.1:p.Gly416=
XM_011515782.1:c.-3-225G=	XP_011514084.1:n.-3-225G=
XM_011515782.2:c.-3-225G=	XP_011514084.1:n.-3-225G=
XM_017011739.1:c.797G=	XP_016867228.1:p.Gly266=
XM_017011740.1:c.797G=	XP_016867229.1:p.Gly266=
NM_000083.3:c.1247G= MANE Select	NP_000074.3:p.Gly416=
NR_046453.2:n.1352G=