Canonical Allele Identifier: CA369643774

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143332740-C-A
• MyVariant Identifiers: chr7:g.143029833C>A (hg19) ; chr7:g.143332740C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332740C>A , CM000669.2:g.143332740C>A	GRCh38
NC_000007.13:g.143029833C>A , CM000669.1:g.143029833C>A	GRCh37
NC_000007.12:g.142739955C>A	NCBI36
NG_009815.1:g.21615C>A
NG_009815.2:g.21615C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1268C>A	ENSP00000498052.2:p.Ala423Asp
ENST00000343257.7:c.1268C>A MANE Select	ENSP00000339867.2:p.Ala423Asp
ENST00000432192.6:c.1092C>A
ENST00000343257.6:c.1268C>A	ENSP00000339867.2:p.Ala423Asp
NM_000083.2:c.1268C>A	NP_000074.2:p.Ala423Asp
NR_046453.1:n.1341+237C>A
XM_011515781.1:c.1292C>A	XP_011514083.1:p.Ala431Asp
XM_011515782.1:c.14C>A	XP_011514084.1:p.Ala5Asp
XM_011515782.2:c.14C>A	XP_011514084.1:p.Ala5Asp
XM_017011739.1:c.842C>A	XP_016867228.1:p.Ala281Asp
XM_017011740.1:c.818C>A	XP_016867229.1:p.Ala273Asp
NM_000083.3:c.1268C>A MANE Select	NP_000074.3:p.Ala423Asp
NR_046453.2:n.1356+237C>A