Canonical Allele Identifier: CA168221438

Gene: CLCN1

Linked Data

• dbSNP Id: rs541215847
• gnomAD v3: 7-143341782-A-G
• gnomAD v4: 7-143341782-A-G
• MyVariant Identifiers: chr7:g.143038875A>G (hg19) ; chr7:g.143341782A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143341782A>G , CM000669.2:g.143341782A>G	GRCh38
NC_000007.13:g.143038875A>G , CM000669.1:g.143038875A>G	GRCh37
NC_000007.12:g.142748997A>G	NCBI36
NG_009815.1:g.30657A>G
NG_009815.2:g.30657A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1583-147A>G	ENSP00000498052.2:n.1583-147A>G
ENST00000343257.7:c.1583-147A>G MANE Select	ENSP00000339867.2:n.1583-147A>G
ENST00000432192.6:c.1407-147A>G
ENST00000343257.6:c.1583-147A>G	ENSP00000339867.2:n.1583-147A>G
NM_000083.2:c.1583-147A>G	NP_000074.2:n.1583-147A>G
NR_046453.1:n.1523-147A>G
XM_011515781.1:c.1607-147A>G	XP_011514083.1:n.1607-147A>G
XM_011515782.1:c.329-147A>G	XP_011514084.1:n.329-147A>G
XM_011515782.2:c.329-147A>G	XP_011514084.1:n.329-147A>G
XM_017011739.1:c.1157-147A>G	XP_016867228.1:n.1157-147A>G
XM_017011740.1:c.1133-147A>G	XP_016867229.1:n.1133-147A>G
NM_000083.3:c.1583-147A>G MANE Select	NP_000074.3:n.1583-147A>G
NR_046453.2:n.1538-147A>G