Canonical Allele Identifier: CA369684985

Gene: CLCN1

Linked Data

• ClinVar Variation Id: 2006316
• ClinVar RCV Id: RCV002811683
• dbSNP Id: rs1304529237
• gnomAD v2: 7-143018922-G-A
• gnomAD v4: 7-143321829-G-A
• MyVariant Identifiers: chr7:g.143018922G>A (hg19) ; chr7:g.143321829G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321829G>A , CM000669.2:g.143321829G>A	GRCh38
NC_000007.13:g.143018922G>A , CM000669.1:g.143018922G>A	GRCh37
NC_000007.12:g.142729044G>A	NCBI36
NG_009815.1:g.10704G>A
NG_009815.2:g.10704G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.677G>A	ENSP00000498052.2:p.Gly226Asp
ENST00000343257.7:c.677G>A MANE Select	ENSP00000339867.2:p.Gly226Asp
ENST00000432192.6:c.445G>A
ENST00000455478.6:c.131G>A	ENSP00000400027.2:p.Gly44Asp
ENST00000650516.1:c.677G>A	ENSP00000498052.1:p.Gly226Asp
ENST00000343257.6:c.677G>A	ENSP00000339867.2:p.Gly226Asp
ENST00000432192.5:c.135G>A
ENST00000455478.5:c.135G>A
ENST00000495612.1:n.135G>A
NM_000083.2:c.677G>A	NP_000074.2:p.Gly226Asp
NR_046453.1:n.764G>A
XM_011515781.1:c.677G>A	XP_011514083.1:p.Gly226Asp
XM_017011739.1:c.384G>A	XP_016867228.1:p.Trp128Ter
XM_017011740.1:c.384G>A	XP_016867229.1:p.Trp128Ter
NM_000083.3:c.677G>A MANE Select	NP_000074.3:p.Gly226Asp
NR_046453.2:n.779G>A