Canonical Allele Identifier: CA458282905

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143036629A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339536A>G , CM000669.2:g.143339536A>G	GRCh38
NC_000007.13:g.143036629A>G , CM000669.1:g.143036629A>G	GRCh37
NC_000007.12:g.142746751A>G	NCBI36
NG_009815.1:g.28411A>G
NG_009815.2:g.28411A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1497A>G	ENSP00000498052.2:p.Gly499=
ENST00000343257.7:c.1497A>G MANE Select	ENSP00000339867.2:p.Gly499=
ENST00000432192.6:c.1321A>G
ENST00000343257.6:c.1497A>G	ENSP00000339867.2:p.Gly499=
NM_000083.2:c.1497A>G	NP_000074.2:p.Gly499=
NR_046453.1:n.1437A>G
XM_011515781.1:c.1521A>G	XP_011514083.1:p.Gly507=
XM_011515782.1:c.243A>G	XP_011514084.1:p.Gly81=
XM_011515782.2:c.243A>G	XP_011514084.1:p.Gly81=
XM_017011739.1:c.1071A>G	XP_016867228.1:p.Gly357=
XM_017011740.1:c.1047A>G	XP_016867229.1:p.Gly349=
NM_000083.3:c.1497A>G MANE Select	NP_000074.3:p.Gly499=
NR_046453.2:n.1452A>G