Canonical Allele Identifier: CA1748881693
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143321743A= , CM000669.2:g.143321743A= GRCh38
NC_000007.13:g.143018836A= , CM000669.1:g.143018836A= GRCh37
NC_000007.12:g.142728958A= NCBI36
NG_009815.1:g.10618A=
NG_009815.2:g.10618A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.591A= ENSP00000498052.2:p.Ile197=
ENST00000343257.7:c.591A= MANE Select ENSP00000339867.2:p.Ile197=
ENST00000432192.6:c.359A=
ENST00000455478.6:c.45A= ENSP00000400027.2:p.Ile15=
ENST00000650516.1:c.591A= ENSP00000498052.1:p.Ile197=
ENST00000343257.6:c.591A= ENSP00000339867.2:p.Ile197=
ENST00000432192.5:c.49A=
ENST00000455478.5:c.49A=
ENST00000495612.1:n.49A=
NM_000083.2:c.591A= NP_000074.2:p.Ile197=
NR_046453.1:n.678A=
XM_011515781.1:c.591A= XP_011514083.1:p.Ile197=
XM_017011739.1:c.298A= XP_016867228.1:p.Thr100=
XM_017011740.1:c.298A= XP_016867229.1:p.Thr100=
NM_000083.3:c.591A= MANE Select NP_000074.3:p.Ile197=
NR_046453.2:n.693A=