Canonical Allele Identifier: CA1732747159
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689032T= , CM000669.2:g.107689032T= GRCh38
NC_000007.13:g.107329477T= , CM000669.1:g.107329477T= GRCh37
NC_000007.12:g.107116713T= NCBI36
NG_008489.1:g.33398T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1002-21T= MANE Select ENSP00000494017.1:n.1002-21T=
ENST00000265715.7:c.1002-21T= ENSP00000265715.3:n.1002-21T=
NM_000441.1:c.1002-21T= NP_000432.1:n.1002-21T=
XM_005250425.1:c.1002-21T= XP_005250482.1:n.1002-21T=
XM_006716025.2:c.1002-21T= XP_006716088.1:n.1002-21T=
XM_005250425.2:c.1002-21T= XP_005250482.1:n.1002-21T=
XM_006716025.3:c.1002-21T= XP_006716088.1:n.1002-21T=
XM_017012318.1:c.1002-21T= XP_016867807.1:n.1002-21T=
NM_000441.2:c.1002-21T= MANE Select NP_000432.1:n.1002-21T=
Search 100 bp 5'
Search 100 bp 3'