Canonical Allele Identifier: CA1732745761
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107674065T= , CM000669.2:g.107674065T= GRCh38
NC_000007.13:g.107314510T= , CM000669.1:g.107314510T= GRCh37
NC_000007.12:g.107101746T= NCBI36
NG_008489.1:g.18431T=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.416-99T= MANE Select ENSP00000494017.1:n.416-99T=
ENST00000265715.7:c.416-99T= ENSP00000265715.3:n.416-99T=
NM_000441.1:c.416-99T= NP_000432.1:n.416-99T=
XM_005250425.1:c.416-99T= XP_005250482.1:n.416-99T=
XM_006716025.2:c.416-99T= XP_006716088.1:n.416-99T=
XM_005250425.2:c.416-99T= XP_005250482.1:n.416-99T=
XM_006716025.3:c.416-99T= XP_006716088.1:n.416-99T=
XM_017012318.1:c.416-99T= XP_016867807.1:n.416-99T=
NM_000441.2:c.416-99T= MANE Select NP_000432.1:n.416-99T=
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