Canonical Allele Identifier: CA1732745817
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107674139A= , CM000669.2:g.107674139A= GRCh38
NC_000007.13:g.107314584A= , CM000669.1:g.107314584A= GRCh37
NC_000007.12:g.107101820A= NCBI36
NG_008489.1:g.18505A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.416-25A= MANE Select ENSP00000494017.1:n.416-25A=
ENST00000265715.7:c.416-25A= ENSP00000265715.3:n.416-25A=
NM_000441.1:c.416-25A= NP_000432.1:n.416-25A=
XM_005250425.1:c.416-25A= XP_005250482.1:n.416-25A=
XM_006716025.2:c.416-25A= XP_006716088.1:n.416-25A=
XM_005250425.2:c.416-25A= XP_005250482.1:n.416-25A=
XM_006716025.3:c.416-25A= XP_006716088.1:n.416-25A=
XM_017012318.1:c.416-25A= XP_016867807.1:n.416-25A=
NM_000441.2:c.416-25A= MANE Select NP_000432.1:n.416-25A=
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