Canonical Allele Identifier: CA458280523

Gene: CLCN1

Linked Data

• dbSNP Id: rs1802699644
• MyVariant Identifiers: chr7:g.143027870C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330777C>T , CM000669.2:g.143330777C>T	GRCh38
NC_000007.13:g.143027870C>T , CM000669.1:g.143027870C>T	GRCh37
NC_000007.12:g.142737992C>T	NCBI36
NG_009815.1:g.19652C>T
NG_009815.2:g.19652C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.859C>T	ENSP00000498052.2:p.Leu287=
ENST00000343257.7:c.859C>T MANE Select	ENSP00000339867.2:p.Leu287=
ENST00000432192.6:c.683C>T
ENST00000455478.6:c.447C>T	ENSP00000400027.2:n.447C>T
ENST00000650516.1:c.859C>T	ENSP00000498052.1:p.Leu287=
ENST00000343257.6:c.859C>T	ENSP00000339867.2:p.Leu287=
ENST00000432192.5:c.373C>T
ENST00000455478.5:c.451C>T
ENST00000495612.1:n.160C>T
NM_000083.2:c.859C>T	NP_000074.2:p.Leu287=
NR_046453.1:n.949C>T
XM_011515781.1:c.859C>T	XP_011514083.1:p.Leu287=
XM_017011739.1:c.409C>T	XP_016867228.1:p.Leu137=
XM_017011740.1:c.409C>T	XP_016867229.1:p.Leu137=
NM_000083.3:c.859C>T MANE Select	NP_000074.3:p.Leu287=
NR_046453.2:n.964C>T