Canonical Allele Identifier: CA369646691

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039186C>G (hg19) ; chr7:g.143342093C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342093C>G , CM000669.2:g.143342093C>G	GRCh38
NC_000007.13:g.143039186C>G , CM000669.1:g.143039186C>G	GRCh37
NC_000007.12:g.142749308C>G	NCBI36
NG_009815.1:g.30968C>G
NG_009815.2:g.30968C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1747C>G	ENSP00000498052.2:p.Gln583Glu
ENST00000343257.7:c.1747C>G MANE Select	ENSP00000339867.2:p.Gln583Glu
ENST00000432192.6:c.1571C>G
ENST00000343257.6:c.1747C>G	ENSP00000339867.2:p.Gln583Glu
NM_000083.2:c.1747C>G	NP_000074.2:p.Gln583Glu
NR_046453.1:n.1687C>G
XM_011515781.1:c.1771C>G	XP_011514083.1:p.Gln591Glu
XM_011515782.1:c.493C>G	XP_011514084.1:p.Gln165Glu
XM_011515782.2:c.493C>G	XP_011514084.1:p.Gln165Glu
XM_017011739.1:c.1321C>G	XP_016867228.1:p.Gln441Glu
XM_017011740.1:c.1297C>G	XP_016867229.1:p.Gln433Glu
NM_000083.3:c.1747C>G MANE Select	NP_000074.3:p.Gln583Glu
NR_046453.2:n.1702C>G