Canonical Allele Identifier: CA2715583578
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs2129319960
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710205_107710206insCTC , CM000669.2:g.107710205_107710206insCTC GRCh38
NC_000007.13:g.107350650_107350651insCTC , CM000669.1:g.107350650_107350651insCTC GRCh37
NC_000007.12:g.107137886_107137887insCTC NCBI36
NG_008489.1:g.54571_54572insCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2235+6_2235+7insCTC MANE Select ENSP00000494017.1:n.2235+6_2235+7insCTC
ENST00000644846.1:c.891+6_891+7insCTC
ENST00000265715.7:c.2235+6_2235+7insCTC ENSP00000265715.3:n.2235+6_2235+7insCTC
ENST00000492030.2:n.421+6_421+7insCTC
NM_000441.1:c.2235+6_2235+7insCTC NP_000432.1:n.2235+6_2235+7insCTC
XM_005250425.1:c.2235+6_2235+7insCTC XP_005250482.1:n.2235+6_2235+7insCTC
XM_005250425.2:c.2235+6_2235+7insCTC XP_005250482.1:n.2235+6_2235+7insCTC
XM_017012318.1:c.2157+6_2157+7insCTC XP_016867807.1:n.2157+6_2157+7insCTC
NM_000441.2:c.2235+6_2235+7insCTC MANE Select NP_000432.1:n.2235+6_2235+7insCTC
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