Canonical Allele Identifier: CA1748894076

Gene: CLCN1

Linked Data

• dbSNP Id: rs1803101254
• gnomAD v4: 7-143342286-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342286G>A , CM000669.2:g.143342286G>A	GRCh38
NC_000007.13:g.143039379G>A , CM000669.1:g.143039379G>A	GRCh37
NC_000007.12:g.142749501G>A	NCBI36
NG_009815.1:g.31161G>A
NG_009815.2:g.31161G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1797-86G>A	ENSP00000498052.2:n.1797-86G>A
ENST00000343257.7:c.1797-86G>A MANE Select	ENSP00000339867.2:n.1797-86G>A
ENST00000432192.6:c.1621-86G>A
ENST00000343257.6:c.1797-86G>A	ENSP00000339867.2:n.1797-86G>A
NM_000083.2:c.1797-86G>A	NP_000074.2:n.1797-86G>A
NR_046453.1:n.1737-86G>A
XM_011515781.1:c.1821-86G>A	XP_011514083.1:n.1821-86G>A
XM_011515782.1:c.543-86G>A	XP_011514084.1:n.543-86G>A
XM_011515782.2:c.543-86G>A	XP_011514084.1:n.543-86G>A
XM_017011739.1:c.1371-86G>A	XP_016867228.1:n.1371-86G>A
XM_017011740.1:c.1347-86G>A	XP_016867229.1:n.1347-86G>A
NM_000083.3:c.1797-86G>A MANE Select	NP_000074.3:n.1797-86G>A
NR_046453.2:n.1752-86G>A