Canonical Allele Identifier: CA369646394

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039049C>G (hg19) ; chr7:g.143341956C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143341956C>G , CM000669.2:g.143341956C>G	GRCh38
NC_000007.13:g.143039049C>G , CM000669.1:g.143039049C>G	GRCh37
NC_000007.12:g.142749171C>G	NCBI36
NG_009815.1:g.30831C>G
NG_009815.2:g.30831C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1610C>G	ENSP00000498052.2:p.Ser537Cys
ENST00000343257.7:c.1610C>G MANE Select	ENSP00000339867.2:p.Ser537Cys
ENST00000432192.6:c.1434C>G
ENST00000343257.6:c.1610C>G	ENSP00000339867.2:p.Ser537Cys
NM_000083.2:c.1610C>G	NP_000074.2:p.Ser537Cys
NR_046453.1:n.1550C>G
XM_011515781.1:c.1634C>G	XP_011514083.1:p.Ser545Cys
XM_011515782.1:c.356C>G	XP_011514084.1:p.Ser119Cys
XM_011515782.2:c.356C>G	XP_011514084.1:p.Ser119Cys
XM_017011739.1:c.1184C>G	XP_016867228.1:p.Ser395Cys
XM_017011740.1:c.1160C>G	XP_016867229.1:p.Ser387Cys
NM_000083.3:c.1610C>G MANE Select	NP_000074.3:p.Ser537Cys
NR_046453.2:n.1565C>G