Canonical Allele Identifier: CA1732751131
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710028_107710029delinsCA , CM000669.2:g.107710028_107710029delinsCA GRCh38
NC_000007.13:g.107350473_107350474delinsCA , CM000669.1:g.107350473_107350474delinsCA GRCh37
NC_000007.12:g.107137709_107137710delinsCA NCBI36
NG_008489.1:g.54394_54395delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2090-26_2090-25delinsCA MANE Select ENSP00000494017.1:n.2090-26_2090-25delinsCA
ENST00000644846.1:c.746-26_746-25delinsCA
ENST00000265715.7:c.2090-26_2090-25delinsCA ENSP00000265715.3:n.2090-26_2090-25delinsCA
ENST00000492030.2:n.377-127_377-126delinsCA
NM_000441.1:c.2090-26_2090-25delinsCA NP_000432.1:n.2090-26_2090-25delinsCA
XM_005250425.1:c.2090-26_2090-25delinsCA XP_005250482.1:n.2090-26_2090-25delinsCA
XM_005250425.2:c.2090-26_2090-25delinsCA XP_005250482.1:n.2090-26_2090-25delinsCA
XM_017012318.1:c.2012-26_2012-25delinsCA XP_016867807.1:n.2012-26_2012-25delinsCA
NM_000441.2:c.2090-26_2090-25delinsCA MANE Select NP_000432.1:n.2090-26_2090-25delinsCA
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