Canonical Allele Identifier: CA1748884074
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143324335C= , CM000669.2:g.143324335C= GRCh38
NC_000007.13:g.143021428C= , CM000669.1:g.143021428C= GRCh37
NC_000007.12:g.142731550C= NCBI36
NG_009815.1:g.13210C=
NG_009815.2:g.13210C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650516.2:c.853+438C= ENSP00000498052.2:n.853+438C=
ENST00000343257.7:c.775-79C= MANE Select ENSP00000339867.2:n.775-79C=
ENST00000432192.6:c.599-79C=
ENST00000455478.6:c.363-79C= ENSP00000400027.2:n.363-79C=
ENST00000650516.1:c.853+438C= ENSP00000498052.1:n.853+438C=
ENST00000343257.6:c.775-79C= ENSP00000339867.2:n.775-79C=
ENST00000432192.5:c.289-79C=
ENST00000455478.5:c.367-79C=
ENST00000495612.1:n.154+2487C=
NM_000083.2:c.775-79C= NP_000074.2:n.775-79C=
NR_046453.1:n.862-76C=
XM_011515781.1:c.853+438C= XP_011514083.1:n.853+438C=
XM_017011739.1:c.403+2487C= XP_016867228.1:n.403+2487C=
XM_017011740.1:c.403+2487C= XP_016867229.1:n.403+2487C=
NM_000083.3:c.775-79C= MANE Select NP_000074.3:n.775-79C=
NR_046453.2:n.877-76C=