Canonical Allele Identifier: CA369645331

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143339284-C-A
• MyVariant Identifiers: chr7:g.143036377C>A (hg19) ; chr7:g.143339284C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339284C>A , CM000669.2:g.143339284C>A	GRCh38
NC_000007.13:g.143036377C>A , CM000669.1:g.143036377C>A	GRCh37
NC_000007.12:g.142746499C>A	NCBI36
NG_009815.1:g.28159C>A
NG_009815.2:g.28159C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1433C>A	ENSP00000498052.2:p.Pro478His
ENST00000343257.7:c.1433C>A MANE Select	ENSP00000339867.2:p.Pro478His
ENST00000432192.6:c.1257C>A
ENST00000343257.6:c.1433C>A	ENSP00000339867.2:p.Pro478His
NM_000083.2:c.1433C>A	NP_000074.2:p.Pro478His
NR_046453.1:n.1373C>A
XM_011515781.1:c.1457C>A	XP_011514083.1:p.Pro486His
XM_011515782.1:c.179C>A	XP_011514084.1:p.Pro60His
XM_011515782.2:c.179C>A	XP_011514084.1:p.Pro60His
XM_017011739.1:c.1007C>A	XP_016867228.1:p.Pro336His
XM_017011740.1:c.983C>A	XP_016867229.1:p.Pro328His
NM_000083.3:c.1433C>A MANE Select	NP_000074.3:p.Pro478His
NR_046453.2:n.1388C>A