Canonical Allele Identifier: CA369683875

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018549C>G (hg19) ; chr7:g.143321456C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321456C>G , CM000669.2:g.143321456C>G	GRCh38
NC_000007.13:g.143018549C>G , CM000669.1:g.143018549C>G	GRCh37
NC_000007.12:g.142728671C>G	NCBI36
NG_009815.1:g.10331C>G
NG_009815.2:g.10331C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.525C>G	ENSP00000498052.2:p.Ser175Arg
ENST00000343257.7:c.525C>G MANE Select	ENSP00000339867.2:p.Ser175Arg
ENST00000432192.6:c.293C>G
ENST00000650516.1:c.525C>G	ENSP00000498052.1:p.Ser175Arg
ENST00000343257.6:c.525C>G	ENSP00000339867.2:p.Ser175Arg
NM_000083.2:c.525C>G	NP_000074.2:p.Ser175Arg
NR_046453.1:n.612C>G
XM_011515781.1:c.525C>G	XP_011514083.1:p.Ser175Arg
XM_017011739.1:c.232C>G	XP_016867228.1:p.Arg78Gly
XM_017011740.1:c.232C>G	XP_016867229.1:p.Arg78Gly
NM_000083.3:c.525C>G MANE Select	NP_000074.3:p.Ser175Arg
NR_046453.2:n.627C>G