Canonical Allele Identifier: CA2579050871

Gene: CLCN1

Linked Data

• ClinVar Variation Id: 2923175
• ClinVar RCV Id: RCV003780293
• gnomAD v4: 7-143342149-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342149G>C , CM000669.2:g.143342149G>C	GRCh38
NC_000007.13:g.143039242G>C , CM000669.1:g.143039242G>C	GRCh37
NC_000007.12:g.142749364G>C	NCBI36
NG_009815.1:g.31024G>C
NG_009815.2:g.31024G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1796+7G>C	ENSP00000498052.2:n.1796+7G>C
ENST00000343257.7:c.1796+7G>C MANE Select	ENSP00000339867.2:n.1796+7G>C
ENST00000432192.6:c.1620+7G>C
ENST00000343257.6:c.1796+7G>C	ENSP00000339867.2:n.1796+7G>C
NM_000083.2:c.1796+7G>C	NP_000074.2:n.1796+7G>C
NR_046453.1:n.1736+7G>C
XM_011515781.1:c.1820+7G>C	XP_011514083.1:n.1820+7G>C
XM_011515782.1:c.542+7G>C	XP_011514084.1:n.542+7G>C
XM_011515782.2:c.542+7G>C	XP_011514084.1:n.542+7G>C
XM_017011739.1:c.1370+7G>C	XP_016867228.1:n.1370+7G>C
XM_017011740.1:c.1346+7G>C	XP_016867229.1:n.1346+7G>C
NM_000083.3:c.1796+7G>C MANE Select	NP_000074.3:n.1796+7G>C
NR_046453.2:n.1751+7G>C