Canonical Allele Identifier: CA458288683

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143047681C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143350588C>G , CM000669.2:g.143350588C>G	GRCh38
NC_000007.13:g.143047681C>G , CM000669.1:g.143047681C>G	GRCh37
NC_000007.12:g.142757803C>G	NCBI36
NG_009815.1:g.39463C>G
NG_009815.2:g.39463C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2529C>G	ENSP00000498052.2:p.Leu843=
ENST00000343257.7:c.2529C>G MANE Select	ENSP00000339867.2:p.Leu843=
ENST00000432192.6:c.2353C>G
ENST00000343257.6:c.2529C>G	ENSP00000339867.2:p.Leu843=
NM_000083.2:c.2529C>G	NP_000074.2:p.Leu843=
NR_046453.1:n.2469C>G
XM_011515781.1:c.2553C>G	XP_011514083.1:p.Leu851=
XM_011515782.1:c.1275C>G	XP_011514084.1:p.Leu425=
XM_011515782.2:c.1275C>G	XP_011514084.1:p.Leu425=
XM_017011739.1:c.2103C>G	XP_016867228.1:p.Leu701=
XM_017011740.1:c.2079C>G	XP_016867229.1:p.Leu693=
NM_000083.3:c.2529C>G MANE Select	NP_000074.3:p.Leu843=
NR_046453.2:n.2484C>G