Canonical Allele Identifier: CA369646777

Gene: CLCN1

Linked Data

• ClinVar Variation Id: 639175
• ClinVar RCV Id: RCV000791909
• dbSNP Id: rs1586510870
• gnomAD v4: 7-143342130-G-A
• MyVariant Identifiers: chr7:g.143039223G>A (hg19) ; chr7:g.143342130G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342130G>A , CM000669.2:g.143342130G>A	GRCh38
NC_000007.13:g.143039223G>A , CM000669.1:g.143039223G>A	GRCh37
NC_000007.12:g.142749345G>A	NCBI36
NG_009815.1:g.31005G>A
NG_009815.2:g.31005G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1784G>A	ENSP00000498052.2:p.Trp595Ter
ENST00000343257.7:c.1784G>A MANE Select	ENSP00000339867.2:p.Trp595Ter
ENST00000432192.6:c.1608G>A
ENST00000343257.6:c.1784G>A	ENSP00000339867.2:p.Trp595Ter
NM_000083.2:c.1784G>A	NP_000074.2:p.Trp595Ter
NR_046453.1:n.1724G>A
XM_011515781.1:c.1808G>A	XP_011514083.1:p.Trp603Ter
XM_011515782.1:c.530G>A	XP_011514084.1:p.Trp177Ter
XM_011515782.2:c.530G>A	XP_011514084.1:p.Trp177Ter
XM_017011739.1:c.1358G>A	XP_016867228.1:p.Trp453Ter
XM_017011740.1:c.1334G>A	XP_016867229.1:p.Trp445Ter
NM_000083.3:c.1784G>A MANE Select	NP_000074.3:p.Trp595Ter
NR_046453.2:n.1739G>A