Canonical Allele Identifier: CA1732755273
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715366G= , CM000669.2:g.107715366G= GRCh38
NC_000007.13:g.107355811G= , CM000669.1:g.107355811G= GRCh37
NC_000007.12:g.107143047G= NCBI36
NG_008489.1:g.59732G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2320-57G= MANE Select ENSP00000494017.1:n.2320-57G=
ENST00000644846.1:c.976-57G=
ENST00000265715.7:c.2320-57G= ENSP00000265715.3:n.2320-57G=
ENST00000492030.2:n.506-57G=
NM_000441.1:c.2320-57G= NP_000432.1:n.2320-57G=
XM_005250425.1:c.2320-57G= XP_005250482.1:n.2320-57G=
XM_005250425.2:c.2320-57G= XP_005250482.1:n.2320-57G=
XM_017012318.1:c.2242-57G= XP_016867807.1:n.2242-57G=
NM_000441.2:c.2320-57G= MANE Select NP_000432.1:n.2320-57G=
Search 100 bp 5'
Search 100 bp 3'