Canonical Allele Identifier: CA1748888879
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143330764C= , CM000669.2:g.143330764C= GRCh38
NC_000007.13:g.143027857C= , CM000669.1:g.143027857C= GRCh37
NC_000007.12:g.142737979C= NCBI36
NG_009815.1:g.19639C=
NG_009815.2:g.19639C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.854-8C= ENSP00000498052.2:n.854-8C=
ENST00000343257.7:c.854-8C= MANE Select ENSP00000339867.2:n.854-8C=
ENST00000432192.6:c.678-8C=
ENST00000455478.6:c.442-8C= ENSP00000400027.2:n.442-8C=
ENST00000650516.1:c.854-8C= ENSP00000498052.1:n.854-8C=
ENST00000343257.6:c.854-8C= ENSP00000339867.2:n.854-8C=
ENST00000432192.5:c.368-8C=
ENST00000455478.5:c.446-8C=
ENST00000495612.1:n.155-8C=
NM_000083.2:c.854-8C= NP_000074.2:n.854-8C=
NR_046453.1:n.944-8C=
XM_011515781.1:c.854-8C= XP_011514083.1:n.854-8C=
XM_017011739.1:c.404-8C= XP_016867228.1:n.404-8C=
XM_017011740.1:c.404-8C= XP_016867229.1:n.404-8C=
NM_000083.3:c.854-8C= MANE Select NP_000074.3:n.854-8C=
NR_046453.2:n.959-8C=