Canonical Allele Identifier: CA2684461011
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107674073-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107674073A>T , CM000669.2:g.107674073A>T GRCh38
NC_000007.13:g.107314518A>T , CM000669.1:g.107314518A>T GRCh37
NC_000007.12:g.107101754A>T NCBI36
NG_008489.1:g.18439A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.416-91A>T MANE Select ENSP00000494017.1:n.416-91A>T
ENST00000265715.7:c.416-91A>T ENSP00000265715.3:n.416-91A>T
NM_000441.1:c.416-91A>T NP_000432.1:n.416-91A>T
XM_005250425.1:c.416-91A>T XP_005250482.1:n.416-91A>T
XM_006716025.2:c.416-91A>T XP_006716088.1:n.416-91A>T
XM_005250425.2:c.416-91A>T XP_005250482.1:n.416-91A>T
XM_006716025.3:c.416-91A>T XP_006716088.1:n.416-91A>T
XM_017012318.1:c.416-91A>T XP_016867807.1:n.416-91A>T
NM_000441.2:c.416-91A>T MANE Select NP_000432.1:n.416-91A>T
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