Canonical Allele Identifier: CA1748889776

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332771G= , CM000669.2:g.143332771G=	GRCh38
NC_000007.13:g.143029864G= , CM000669.1:g.143029864G=	GRCh37
NC_000007.12:g.142739986G=	NCBI36
NG_009815.1:g.21646G=
NG_009815.2:g.21646G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1299G=	ENSP00000498052.2:p.Trp433=
ENST00000343257.7:c.1299G= MANE Select	ENSP00000339867.2:p.Trp433=
ENST00000432192.6:c.1123G=
ENST00000343257.6:c.1299G=	ENSP00000339867.2:p.Trp433=
NM_000083.2:c.1299G=	NP_000074.2:p.Trp433=
NR_046453.1:n.1341+268G=
XM_011515781.1:c.1323G=	XP_011514083.1:p.Trp441=
XM_011515782.1:c.45G=	XP_011514084.1:p.Trp15=
XM_011515782.2:c.45G=	XP_011514084.1:p.Trp15=
XM_017011739.1:c.873G=	XP_016867228.1:p.Trp291=
XM_017011740.1:c.849G=	XP_016867229.1:p.Trp283=
NM_000083.3:c.1299G= MANE Select	NP_000074.3:p.Trp433=
NR_046453.2:n.1356+268G=