Canonical Allele Identifier: CA369646729

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143342111-T-G
• MyVariant Identifiers: chr7:g.143039204T>G (hg19) ; chr7:g.143342111T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342111T>G , CM000669.2:g.143342111T>G	GRCh38
NC_000007.13:g.143039204T>G , CM000669.1:g.143039204T>G	GRCh37
NC_000007.12:g.142749326T>G	NCBI36
NG_009815.1:g.30986T>G
NG_009815.2:g.30986T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1765T>G	ENSP00000498052.2:p.Tyr589Asp
ENST00000343257.7:c.1765T>G MANE Select	ENSP00000339867.2:p.Tyr589Asp
ENST00000432192.6:c.1589T>G
ENST00000343257.6:c.1765T>G	ENSP00000339867.2:p.Tyr589Asp
NM_000083.2:c.1765T>G	NP_000074.2:p.Tyr589Asp
NR_046453.1:n.1705T>G
XM_011515781.1:c.1789T>G	XP_011514083.1:p.Tyr597Asp
XM_011515782.1:c.511T>G	XP_011514084.1:p.Tyr171Asp
XM_011515782.2:c.511T>G	XP_011514084.1:p.Tyr171Asp
XM_017011739.1:c.1339T>G	XP_016867228.1:p.Tyr447Asp
XM_017011740.1:c.1315T>G	XP_016867229.1:p.Tyr439Asp
NM_000083.3:c.1765T>G MANE Select	NP_000074.3:p.Tyr589Asp
NR_046453.2:n.1720T>G