Canonical Allele Identifier: CA457103252
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107701931-T-A
MyVariant Identifiers: chr7:g.107342376T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701931T>A , CM000669.2:g.107701931T>A GRCh38
NC_000007.13:g.107342376T>A , CM000669.1:g.107342376T>A GRCh37
NC_000007.12:g.107129612T>A NCBI36
NG_008489.1:g.46297T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1908T>A MANE Select ENSP00000494017.1:p.Ile636=
ENST00000644846.1:c.619T>A
ENST00000265715.7:c.1908T>A ENSP00000265715.3:p.Ile636=
ENST00000492030.2:n.195T>A
NM_000441.1:c.1908T>A NP_000432.1:p.Ile636=
XM_005250425.1:c.1908T>A XP_005250482.1:p.Ile636=
XM_005250425.2:c.1908T>A XP_005250482.1:p.Ile636=
XM_017012318.1:c.1830T>A XP_016867807.1:p.Ile610=
NM_000441.2:c.1908T>A MANE Select NP_000432.1:p.Ile636=
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