Canonical Allele Identifier: CA2684466405
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107689283-TAAAG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689286_107689289del , CM000669.2:g.107689286_107689289del GRCh38
NC_000007.13:g.107329731_107329734del , CM000669.1:g.107329731_107329734del GRCh37
NC_000007.12:g.107116967_107116970del NCBI36
NG_008489.1:g.33652_33655del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+86_1149+89del MANE Select ENSP00000494017.1:n.1149+86_1149+89del
ENST00000265715.7:c.1149+86_1149+89del ENSP00000265715.3:n.1149+86_1149+89del
NM_000441.1:c.1149+86_1149+89del NP_000432.1:n.1149+86_1149+89del
XM_005250425.1:c.1149+86_1149+89del XP_005250482.1:n.1149+86_1149+89del
XM_006716025.2:c.1149+86_1149+89del XP_006716088.1:n.1149+86_1149+89del
XM_005250425.2:c.1149+86_1149+89del XP_005250482.1:n.1149+86_1149+89del
XM_006716025.3:c.1149+86_1149+89del XP_006716088.1:n.1149+86_1149+89del
XM_017012318.1:c.1149+86_1149+89del XP_016867807.1:n.1149+86_1149+89del
NM_000441.2:c.1149+86_1149+89del MANE Select NP_000432.1:n.1149+86_1149+89del
Search 100 bp 5'
Search 100 bp 3'