Canonical Allele Identifier: CA1732741834
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107683438_107683440delinsCTT , CM000669.2:g.107683438_107683440delinsCTT GRCh38
NC_000007.13:g.107323883_107323885delinsCTT , CM000669.1:g.107323883_107323885delinsCTT GRCh37
NC_000007.12:g.107111119_107111121delinsCTT NCBI36
NG_008489.1:g.27804_27806delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.919-17_919-15delinsCTT MANE Select ENSP00000494017.1:n.919-17_919-15delinsCT...
ENST00000265715.7:c.919-17_919-15delinsCTT ENSP00000265715.3:n.919-17_919-15delinsCT...
NM_000441.1:c.919-17_919-15delinsCTT NP_000432.1:n.919-17_919-15delinsCTT
XM_005250425.1:c.919-17_919-15delinsCTT XP_005250482.1:n.919-17_919-15delinsCTT
XM_006716025.2:c.919-17_919-15delinsCTT XP_006716088.1:n.919-17_919-15delinsCTT
XM_005250425.2:c.919-17_919-15delinsCTT XP_005250482.1:n.919-17_919-15delinsCTT
XM_006716025.3:c.919-17_919-15delinsCTT XP_006716088.1:n.919-17_919-15delinsCTT
XM_017012318.1:c.919-17_919-15delinsCTT XP_016867807.1:n.919-17_919-15delinsCTT
NM_000441.2:c.919-17_919-15delinsCTT MANE Select NP_000432.1:n.919-17_919-15delinsCTT
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