Canonical Allele Identifier: CA369653136

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143350575-C-A
• MyVariant Identifiers: chr7:g.143047668C>A (hg19) ; chr7:g.143350575C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143350575C>A , CM000669.2:g.143350575C>A	GRCh38
NC_000007.13:g.143047668C>A , CM000669.1:g.143047668C>A	GRCh37
NC_000007.12:g.142757790C>A	NCBI36
NG_009815.1:g.39450C>A
NG_009815.2:g.39450C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2516C>A	ENSP00000498052.2:p.Thr839Asn
ENST00000343257.7:c.2516C>A MANE Select	ENSP00000339867.2:p.Thr839Asn
ENST00000432192.6:c.2340C>A
ENST00000343257.6:c.2516C>A	ENSP00000339867.2:p.Thr839Asn
NM_000083.2:c.2516C>A	NP_000074.2:p.Thr839Asn
NR_046453.1:n.2456C>A
XM_011515781.1:c.2540C>A	XP_011514083.1:p.Thr847Asn
XM_011515782.1:c.1262C>A	XP_011514084.1:p.Thr421Asn
XM_011515782.2:c.1262C>A	XP_011514084.1:p.Thr421Asn
XM_017011739.1:c.2090C>A	XP_016867228.1:p.Thr697Asn
XM_017011740.1:c.2066C>A	XP_016867229.1:p.Thr689Asn
NM_000083.3:c.2516C>A MANE Select	NP_000074.3:p.Thr839Asn
NR_046453.2:n.2471C>A