Canonical Allele Identifier: CA4537030

Gene: CLCN1

Linked Data

• dbSNP Id: rs770986156
• ExAC: 7:143018911 C / T
• gnomAD v2: 7-143018911-C-T
• gnomAD v4: 7-143321818-C-T
• MyVariant Identifiers: chr7:g.143018911C>T (hg19) ; chr7:g.143321818C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321818C>T , CM000669.2:g.143321818C>T	GRCh38
NC_000007.13:g.143018911C>T , CM000669.1:g.143018911C>T	GRCh37
NC_000007.12:g.142729033C>T	NCBI36
NG_009815.1:g.10693C>T
NG_009815.2:g.10693C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.666C>T	ENSP00000498052.2:p.Gly222=
ENST00000343257.7:c.666C>T MANE Select	ENSP00000339867.2:p.Gly222=
ENST00000432192.6:c.434C>T
ENST00000455478.6:c.120C>T	ENSP00000400027.2:p.Gly40=
ENST00000650516.1:c.666C>T	ENSP00000498052.1:p.Gly222=
ENST00000343257.6:c.666C>T	ENSP00000339867.2:p.Gly222=
ENST00000432192.5:c.124C>T
ENST00000455478.5:c.124C>T
ENST00000495612.1:n.124C>T
NM_000083.2:c.666C>T	NP_000074.2:p.Gly222=
NR_046453.1:n.753C>T
XM_011515781.1:c.666C>T	XP_011514083.1:p.Gly222=
XM_017011739.1:c.373C>T	XP_016867228.1:p.Pro125Ser
XM_017011740.1:c.373C>T	XP_016867229.1:p.Pro125Ser
NM_000083.3:c.666C>T MANE Select	NP_000074.3:p.Gly222=
NR_046453.2:n.768C>T