Canonical Allele Identifier: CA458283227

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039041T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143341948T>G , CM000669.2:g.143341948T>G	GRCh38
NC_000007.13:g.143039041T>G , CM000669.1:g.143039041T>G	GRCh37
NC_000007.12:g.142749163T>G	NCBI36
NG_009815.1:g.30823T>G
NG_009815.2:g.30823T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1602T>G	ENSP00000498052.2:p.Gly534=
ENST00000343257.7:c.1602T>G MANE Select	ENSP00000339867.2:p.Gly534=
ENST00000432192.6:c.1426T>G
ENST00000343257.6:c.1602T>G	ENSP00000339867.2:p.Gly534=
NM_000083.2:c.1602T>G	NP_000074.2:p.Gly534=
NR_046453.1:n.1542T>G
XM_011515781.1:c.1626T>G	XP_011514083.1:p.Gly542=
XM_011515782.1:c.348T>G	XP_011514084.1:p.Gly116=
XM_011515782.2:c.348T>G	XP_011514084.1:p.Gly116=
XM_017011739.1:c.1176T>G	XP_016867228.1:p.Gly392=
XM_017011740.1:c.1152T>G	XP_016867229.1:p.Gly384=
NM_000083.3:c.1602T>G MANE Select	NP_000074.3:p.Gly534=
NR_046453.2:n.1557T>G