Canonical Allele Identifier: CA458282881

Gene: CLCN1

Linked Data

• dbSNP Id: rs1045456680
• MyVariant Identifiers: chr7:g.143036561C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339468C>G , CM000669.2:g.143339468C>G	GRCh38
NC_000007.13:g.143036561C>G , CM000669.1:g.143036561C>G	GRCh37
NC_000007.12:g.142746683C>G	NCBI36
NG_009815.1:g.28343C>G
NG_009815.2:g.28343C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1472-43C>G	ENSP00000498052.2:n.1472-43C>G
ENST00000343257.7:c.1472-43C>G MANE Select	ENSP00000339867.2:n.1472-43C>G
ENST00000432192.6:c.1296-43C>G
ENST00000343257.6:c.1472-43C>G	ENSP00000339867.2:n.1472-43C>G
NM_000083.2:c.1472-43C>G	NP_000074.2:n.1472-43C>G
NR_046453.1:n.1412-43C>G
XM_011515781.1:c.1496-43C>G	XP_011514083.1:n.1496-43C>G
XM_011515782.1:c.218-43C>G	XP_011514084.1:n.218-43C>G
XM_011515782.2:c.218-43C>G	XP_011514084.1:n.218-43C>G
XM_017011739.1:c.1046-43C>G	XP_016867228.1:n.1046-43C>G
XM_017011740.1:c.1022-43C>G	XP_016867229.1:n.1022-43C>G
NM_000083.3:c.1472-43C>G MANE Select	NP_000074.3:n.1472-43C>G
NR_046453.2:n.1427-43C>G