Canonical Allele Identifier: CA1732753665
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107696385C= , CM000669.2:g.107696385C= GRCh38
NC_000007.13:g.107336830C= , CM000669.1:g.107336830C= GRCh37
NC_000007.12:g.107124066C= NCBI36
NG_008489.1:g.40751C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1544+346C= MANE Select ENSP00000494017.1:n.1544+346C=
ENST00000644846.1:c.255+346C=
ENST00000265715.7:c.1544+346C= ENSP00000265715.3:n.1544+346C=
ENST00000477350.5:n.391+346C=
ENST00000480841.5:n.393+346C=
NM_000441.1:c.1544+346C= NP_000432.1:n.1544+346C=
XM_005250425.1:c.1544+346C= XP_005250482.1:n.1544+346C=
XM_005250425.2:c.1544+346C= XP_005250482.1:n.1544+346C=
XM_017012318.1:c.1466+346C= XP_016867807.1:n.1466+346C=
NM_000441.2:c.1544+346C= MANE Select NP_000432.1:n.1544+346C=
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