Canonical Allele Identifier: CA458542498

Gene: CLCN1

Linked Data

• dbSNP Id: rs1413611627
• gnomAD v2: 7-143048962-G-A
• gnomAD v4: 7-143351869-G-A
• MyVariant Identifiers: chr7:g.143048962G>A (hg19) ; chr7:g.143351869G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351869G>A , CM000669.2:g.143351869G>A	GRCh38
NC_000007.13:g.143048962G>A , CM000669.1:g.143048962G>A	GRCh37
NC_000007.12:g.142759084G>A	NCBI36
NG_009815.1:g.40744G>A
NG_009815.2:g.40744G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2871G>A	ENSP00000498052.2:p.Val957=
ENST00000343257.7:c.2871G>A MANE Select	ENSP00000339867.2:p.Val957=
ENST00000343257.6:c.2871G>A	ENSP00000339867.2:p.Val957=
NM_000083.2:c.2871G>A	NP_000074.2:p.Val957=
NR_046453.1:n.2811G>A
XM_011515781.1:c.2895G>A	XP_011514083.1:p.Val965=
XM_011515782.1:c.1617G>A	XP_011514084.1:p.Val539=
XM_011515782.2:c.1617G>A	XP_011514084.1:p.Val539=
XM_017011739.1:c.2445G>A	XP_016867228.1:p.Val815=
XM_017011740.1:c.2421G>A	XP_016867229.1:p.Val807=
NM_000083.3:c.2871G>A MANE Select	NP_000074.3:p.Val957=
NR_046453.2:n.2826G>A