Canonical Allele Identifier: CA2777354970
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689335del , CM000669.2:g.107689335del GRCh38
NC_000007.13:g.107329780del , CM000669.1:g.107329780del GRCh37
NC_000007.12:g.107117016del NCBI36
NG_008489.1:g.33701del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+135del MANE Select ENSP00000494017.1:n.1149+135del
ENST00000265715.7:c.1149+135del ENSP00000265715.3:n.1149+135del
NM_000441.1:c.1149+135del NP_000432.1:n.1149+135del
XM_005250425.1:c.1149+135del XP_005250482.1:n.1149+135del
XM_006716025.2:c.1149+135del XP_006716088.1:n.1149+135del
XM_005250425.2:c.1149+135del XP_005250482.1:n.1149+135del
XM_006716025.3:c.1149+135del XP_006716088.1:n.1149+135del
XM_017012318.1:c.1149+135del XP_016867807.1:n.1149+135del
NM_000441.2:c.1149+135del MANE Select NP_000432.1:n.1149+135del
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