Canonical Allele Identifier: CA369646719

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039198C>G (hg19) ; chr7:g.143342105C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342105C>G , CM000669.2:g.143342105C>G	GRCh38
NC_000007.13:g.143039198C>G , CM000669.1:g.143039198C>G	GRCh37
NC_000007.12:g.142749320C>G	NCBI36
NG_009815.1:g.30980C>G
NG_009815.2:g.30980C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1759C>G	ENSP00000498052.2:p.Leu587Val
ENST00000343257.7:c.1759C>G MANE Select	ENSP00000339867.2:p.Leu587Val
ENST00000432192.6:c.1583C>G
ENST00000343257.6:c.1759C>G	ENSP00000339867.2:p.Leu587Val
NM_000083.2:c.1759C>G	NP_000074.2:p.Leu587Val
NR_046453.1:n.1699C>G
XM_011515781.1:c.1783C>G	XP_011514083.1:p.Leu595Val
XM_011515782.1:c.505C>G	XP_011514084.1:p.Leu169Val
XM_011515782.2:c.505C>G	XP_011514084.1:p.Leu169Val
XM_017011739.1:c.1333C>G	XP_016867228.1:p.Leu445Val
XM_017011740.1:c.1309C>G	XP_016867229.1:p.Leu437Val
NM_000083.3:c.1759C>G MANE Select	NP_000074.3:p.Leu587Val
NR_046453.2:n.1714C>G