Canonical Allele Identifier: CA1748898452
Gene: CLCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143352024G= , CM000669.2:g.143352024G= GRCh38
NC_000007.13:g.143049117G= , CM000669.1:g.143049117G= GRCh37
NC_000007.12:g.142759239G= NCBI36
NG_009815.1:g.40899G=
NG_009815.2:g.40899G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650516.2:c.*59G= ENSP00000498052.2:n.*59G=
ENST00000343257.7:c.*59G= MANE Select ENSP00000339867.2:n.*59G=
ENST00000343257.6:c.*59G= ENSP00000339867.2:n.*59G=
XM_011515781.1:c.*59G= XP_011514083.1:n.*59G=
XM_011515782.1:c.*59G= XP_011514084.1:n.*59G=
NM_000083.3:c.*59G= MANE Select NP_000074.3:n.*59G=
NR_046453.2:n.2981G=
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