Canonical Allele Identifier: CA1630834952
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143321747C= , CM000669.2:g.143321747C= GRCh38
NC_000007.13:g.143018840C= , CM000669.1:g.143018840C= GRCh37
NC_000007.12:g.142728962C= NCBI36
NG_009815.1:g.10622C=
NG_009815.2:g.10622C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.595C= ENSP00000498052.2:p.Arg199=
ENST00000343257.7:c.595C= MANE Select ENSP00000339867.2:p.Arg199=
ENST00000432192.6:c.363C=
ENST00000455478.6:c.49C= ENSP00000400027.2:p.Arg17=
ENST00000650516.1:c.595C= ENSP00000498052.1:p.Arg199=
ENST00000343257.6:c.595C= ENSP00000339867.2:p.Arg199=
ENST00000432192.5:c.53C=
ENST00000455478.5:c.53C=
ENST00000495612.1:n.53C=
NM_000083.2:c.595C= NP_000074.2:p.Arg199=
NR_046453.1:n.682C=
XM_011515781.1:c.595C= XP_011514083.1:p.Arg199=
XM_017011739.1:c.302C= XP_016867228.1:p.Ser101=
XM_017011740.1:c.302C= XP_016867229.1:p.Ser101=
NM_000083.3:c.595C= MANE Select NP_000074.3:p.Arg199=
NR_046453.2:n.697C=