Canonical Allele Identifier: CA1732747130
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689004_107689005delinsAG , CM000669.2:g.107689004_107689005delinsAG GRCh38
NC_000007.13:g.107329449_107329450delinsAG , CM000669.1:g.107329449_107329450delinsAG GRCh37
NC_000007.12:g.107116685_107116686delinsAG NCBI36
NG_008489.1:g.33370_33371delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1002-49_1002-48delinsAG MANE Select ENSP00000494017.1:n.1002-49_1002-48delinsAG
ENST00000265715.7:c.1002-49_1002-48delinsAG ENSP00000265715.3:n.1002-49_1002-48delinsAG
NM_000441.1:c.1002-49_1002-48delinsAG NP_000432.1:n.1002-49_1002-48delinsAG
XM_005250425.1:c.1002-49_1002-48delinsAG XP_005250482.1:n.1002-49_1002-48delinsAG
XM_006716025.2:c.1002-49_1002-48delinsAG XP_006716088.1:n.1002-49_1002-48delinsAG
XM_005250425.2:c.1002-49_1002-48delinsAG XP_005250482.1:n.1002-49_1002-48delinsAG
XM_006716025.3:c.1002-49_1002-48delinsAG XP_006716088.1:n.1002-49_1002-48delinsAG
XM_017012318.1:c.1002-49_1002-48delinsAG XP_016867807.1:n.1002-49_1002-48delinsAG
NM_000441.2:c.1002-49_1002-48delinsAG MANE Select NP_000432.1:n.1002-49_1002-48delinsAG
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