Canonical Allele Identifier: CA458542008

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018513C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321420C>G , CM000669.2:g.143321420C>G	GRCh38
NC_000007.13:g.143018513C>G , CM000669.1:g.143018513C>G	GRCh37
NC_000007.12:g.142728635C>G	NCBI36
NG_009815.1:g.10295C>G
NG_009815.2:g.10295C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.489C>G	ENSP00000498052.2:p.Val163=
ENST00000343257.7:c.489C>G MANE Select	ENSP00000339867.2:p.Val163=
ENST00000432192.6:c.257C>G
ENST00000650516.1:c.489C>G	ENSP00000498052.1:p.Val163=
ENST00000343257.6:c.489C>G	ENSP00000339867.2:p.Val163=
NM_000083.2:c.489C>G	NP_000074.2:p.Val163=
NR_046453.1:n.576C>G
XM_011515781.1:c.489C>G	XP_011514083.1:p.Val163=
XM_017011739.1:c.196C>G	XP_016867228.1:p.Leu66Val
XM_017011740.1:c.196C>G	XP_016867229.1:p.Leu66Val
NM_000083.3:c.489C>G MANE Select	NP_000074.3:p.Val163=
NR_046453.2:n.591C>G