Canonical Allele Identifier: CA369684923

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018910G>T (hg19) ; chr7:g.143321817G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321817G>T , CM000669.2:g.143321817G>T	GRCh38
NC_000007.13:g.143018910G>T , CM000669.1:g.143018910G>T	GRCh37
NC_000007.12:g.142729032G>T	NCBI36
NG_009815.1:g.10692G>T
NG_009815.2:g.10692G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.665G>T	ENSP00000498052.2:p.Gly222Val
ENST00000343257.7:c.665G>T MANE Select	ENSP00000339867.2:p.Gly222Val
ENST00000432192.6:c.433G>T
ENST00000455478.6:c.119G>T	ENSP00000400027.2:p.Gly40Val
ENST00000650516.1:c.665G>T	ENSP00000498052.1:p.Gly222Val
ENST00000343257.6:c.665G>T	ENSP00000339867.2:p.Gly222Val
ENST00000432192.5:c.123G>T
ENST00000455478.5:c.123G>T
ENST00000495612.1:n.123G>T
NM_000083.2:c.665G>T	NP_000074.2:p.Gly222Val
NR_046453.1:n.752G>T
XM_011515781.1:c.665G>T	XP_011514083.1:p.Gly222Val
XM_017011739.1:c.372G>T	XP_016867228.1:p.Gly124=
XM_017011740.1:c.372G>T	XP_016867229.1:p.Gly124=
NM_000083.3:c.665G>T MANE Select	NP_000074.3:p.Gly222Val
NR_046453.2:n.767G>T