Canonical Allele Identifier: CA1732747409
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689199_107689200delinsAG , CM000669.2:g.107689199_107689200delinsAG GRCh38
NC_000007.13:g.107329644_107329645delinsAG , CM000669.1:g.107329644_107329645delinsAG GRCh37
NC_000007.12:g.107116880_107116881delinsAG NCBI36
NG_008489.1:g.33565_33566delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1148_1149delinsAG MANE Select ENSP00000494017.1:p.Gln383=
ENST00000265715.7:c.1148_1149delinsAG ENSP00000265715.3:p.Gln383=
NM_000441.1:c.1148_1149delinsAG NP_000432.1:p.Gln383=
XM_005250425.1:c.1148_1149delinsAG XP_005250482.1:p.Gln383=
XM_006716025.2:c.1148_1149delinsAG XP_006716088.1:p.Gln383=
XM_005250425.2:c.1148_1149delinsAG XP_005250482.1:p.Gln383=
XM_006716025.3:c.1148_1149delinsAG XP_006716088.1:p.Gln383=
XM_017012318.1:c.1148_1149delinsAG XP_016867807.1:p.Gln383=
NM_000441.2:c.1148_1149delinsAG MANE Select NP_000432.1:p.Gln383=
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