Canonical Allele Identifier: CA458283460

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039212T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342119T>A , CM000669.2:g.143342119T>A	GRCh38
NC_000007.13:g.143039212T>A , CM000669.1:g.143039212T>A	GRCh37
NC_000007.12:g.142749334T>A	NCBI36
NG_009815.1:g.30994T>A
NG_009815.2:g.30994T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1773T>A	ENSP00000498052.2:p.Pro591=
ENST00000343257.7:c.1773T>A MANE Select	ENSP00000339867.2:p.Pro591=
ENST00000432192.6:c.1597T>A
ENST00000343257.6:c.1773T>A	ENSP00000339867.2:p.Pro591=
NM_000083.2:c.1773T>A	NP_000074.2:p.Pro591=
NR_046453.1:n.1713T>A
XM_011515781.1:c.1797T>A	XP_011514083.1:p.Pro599=
XM_011515782.1:c.519T>A	XP_011514084.1:p.Pro173=
XM_011515782.2:c.519T>A	XP_011514084.1:p.Pro173=
XM_017011739.1:c.1347T>A	XP_016867228.1:p.Pro449=
XM_017011740.1:c.1323T>A	XP_016867229.1:p.Pro441=
NM_000083.3:c.1773T>A MANE Select	NP_000074.3:p.Pro591=
NR_046453.2:n.1728T>A