Canonical Allele Identifier: CA1748889000
Gene: CLCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143330997G= , CM000669.2:g.143330997G= GRCh38
NC_000007.13:g.143028090G= , CM000669.1:g.143028090G= GRCh37
NC_000007.12:g.142738212G= NCBI36
NG_009815.1:g.19872G=
NG_009815.2:g.19872G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650516.2:c.979+100G= ENSP00000498052.2:n.979+100G=
ENST00000343257.7:c.979+100G= MANE Select ENSP00000339867.2:n.979+100G=
ENST00000432192.6:c.803+100G=
ENST00000343257.6:c.979+100G= ENSP00000339867.2:n.979+100G=
NM_000083.2:c.979+100G= NP_000074.2:n.979+100G=
NR_046453.1:n.1069+100G=
XM_011515781.1:c.979+100G= XP_011514083.1:n.979+100G=
XM_017011739.1:c.529+100G= XP_016867228.1:n.529+100G=
XM_017011740.1:c.529+100G= XP_016867229.1:n.529+100G=
NM_000083.3:c.979+100G= MANE Select NP_000074.3:n.979+100G=
NR_046453.2:n.1084+100G=
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