Canonical Allele Identifier: CA458283456

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039203C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342110C>G , CM000669.2:g.143342110C>G	GRCh38
NC_000007.13:g.143039203C>G , CM000669.1:g.143039203C>G	GRCh37
NC_000007.12:g.142749325C>G	NCBI36
NG_009815.1:g.30985C>G
NG_009815.2:g.30985C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1764C>G	ENSP00000498052.2:p.Pro588=
ENST00000343257.7:c.1764C>G MANE Select	ENSP00000339867.2:p.Pro588=
ENST00000432192.6:c.1588C>G
ENST00000343257.6:c.1764C>G	ENSP00000339867.2:p.Pro588=
NM_000083.2:c.1764C>G	NP_000074.2:p.Pro588=
NR_046453.1:n.1704C>G
XM_011515781.1:c.1788C>G	XP_011514083.1:p.Pro596=
XM_011515782.1:c.510C>G	XP_011514084.1:p.Pro170=
XM_011515782.2:c.510C>G	XP_011514084.1:p.Pro170=
XM_017011739.1:c.1338C>G	XP_016867228.1:p.Pro446=
XM_017011740.1:c.1314C>G	XP_016867229.1:p.Pro438=
NM_000083.3:c.1764C>G MANE Select	NP_000074.3:p.Pro588=
NR_046453.2:n.1719C>G