Canonical Allele Identifier: CA458542314

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143351632-G-A
• MyVariant Identifiers: chr7:g.143048725G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351632G>A , CM000669.2:g.143351632G>A	GRCh38
NC_000007.13:g.143048725G>A , CM000669.1:g.143048725G>A	GRCh37
NC_000007.12:g.142758847G>A	NCBI36
NG_009815.1:g.40507G>A
NG_009815.2:g.40507G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2634G>A	ENSP00000498052.2:p.Val878=
ENST00000343257.7:c.2634G>A MANE Select	ENSP00000339867.2:p.Val878=
ENST00000432192.6:c.2458G>A
ENST00000343257.6:c.2634G>A	ENSP00000339867.2:p.Val878=
NM_000083.2:c.2634G>A	NP_000074.2:p.Val878=
NR_046453.1:n.2574G>A
XM_011515781.1:c.2658G>A	XP_011514083.1:p.Val886=
XM_011515782.1:c.1380G>A	XP_011514084.1:p.Val460=
XM_011515782.2:c.1380G>A	XP_011514084.1:p.Val460=
XM_017011739.1:c.2208G>A	XP_016867228.1:p.Val736=
XM_017011740.1:c.2184G>A	XP_016867229.1:p.Val728=
NM_000083.3:c.2634G>A MANE Select	NP_000074.3:p.Val878=
NR_046453.2:n.2589G>A