Canonical Allele Identifier: CA369683730

Gene: CLCN1

Linked Data

• ClinVar Variation Id: 3068602
• ClinVar RCV Id: RCV003994671
• MyVariant Identifiers: chr7:g.143018526C>G (hg19) ; chr7:g.143321433C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321433C>G , CM000669.2:g.143321433C>G	GRCh38
NC_000007.13:g.143018526C>G , CM000669.1:g.143018526C>G	GRCh37
NC_000007.12:g.142728648C>G	NCBI36
NG_009815.1:g.10308C>G
NG_009815.2:g.10308C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.502C>G	ENSP00000498052.2:p.Pro168Ala
ENST00000343257.7:c.502C>G MANE Select	ENSP00000339867.2:p.Pro168Ala
ENST00000432192.6:c.270C>G
ENST00000650516.1:c.502C>G	ENSP00000498052.1:p.Pro168Ala
ENST00000343257.6:c.502C>G	ENSP00000339867.2:p.Pro168Ala
NM_000083.2:c.502C>G	NP_000074.2:p.Pro168Ala
NR_046453.1:n.589C>G
XM_011515781.1:c.502C>G	XP_011514083.1:p.Pro168Ala
XM_017011739.1:c.209C>G	XP_016867228.1:p.Pro70Arg
XM_017011740.1:c.209C>G	XP_016867229.1:p.Pro70Arg
NM_000083.3:c.502C>G MANE Select	NP_000074.3:p.Pro168Ala
NR_046453.2:n.604C>G