Canonical Allele Identifier: CA369653956

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143351849-T-G
• MyVariant Identifiers: chr7:g.143048942T>G (hg19) ; chr7:g.143351849T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351849T>G , CM000669.2:g.143351849T>G	GRCh38
NC_000007.13:g.143048942T>G , CM000669.1:g.143048942T>G	GRCh37
NC_000007.12:g.142759064T>G	NCBI36
NG_009815.1:g.40724T>G
NG_009815.2:g.40724T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2851T>G	ENSP00000498052.2:p.Leu951Val
ENST00000343257.7:c.2851T>G MANE Select	ENSP00000339867.2:p.Leu951Val
ENST00000343257.6:c.2851T>G	ENSP00000339867.2:p.Leu951Val
NM_000083.2:c.2851T>G	NP_000074.2:p.Leu951Val
NR_046453.1:n.2791T>G
XM_011515781.1:c.2875T>G	XP_011514083.1:p.Leu959Val
XM_011515782.1:c.1597T>G	XP_011514084.1:p.Leu533Val
XM_011515782.2:c.1597T>G	XP_011514084.1:p.Leu533Val
XM_017011739.1:c.2425T>G	XP_016867228.1:p.Leu809Val
XM_017011740.1:c.2401T>G	XP_016867229.1:p.Leu801Val
NM_000083.3:c.2851T>G MANE Select	NP_000074.3:p.Leu951Val
NR_046453.2:n.2806T>G