Canonical Allele Identifier: CA1748888936
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143330868G= , CM000669.2:g.143330868G= GRCh38
NC_000007.13:g.143027961G= , CM000669.1:g.143027961G= GRCh37
NC_000007.12:g.142738083G= NCBI36
NG_009815.1:g.19743G=
NG_009815.2:g.19743G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.950G= ENSP00000498052.2:p.Arg317=
ENST00000343257.7:c.950G= MANE Select ENSP00000339867.2:p.Arg317=
ENST00000432192.6:c.774G=
ENST00000455478.6:c.538G= ENSP00000400027.2:n.538G=
ENST00000650516.1:c.950G= ENSP00000498052.1:p.Arg317=
ENST00000343257.6:c.950G= ENSP00000339867.2:p.Arg317=
ENST00000432192.5:c.464G=
ENST00000455478.5:c.542G=
ENST00000495612.1:n.251G=
NM_000083.2:c.950G= NP_000074.2:p.Arg317=
NR_046453.1:n.1040G=
XM_011515781.1:c.950G= XP_011514083.1:p.Arg317=
XM_017011739.1:c.500G= XP_016867228.1:p.Arg167=
XM_017011740.1:c.500G= XP_016867229.1:p.Arg167=
NM_000083.3:c.950G= MANE Select NP_000074.3:p.Arg317=
NR_046453.2:n.1055G=