Canonical Allele Identifier: CA457090231
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107690135-C-A
MyVariant Identifiers: chr7:g.107330580C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107690135C>A , CM000669.2:g.107690135C>A GRCh38
NC_000007.13:g.107330580C>A , CM000669.1:g.107330580C>A GRCh37
NC_000007.12:g.107117816C>A NCBI36
NG_008489.1:g.34501C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1161C>A MANE Select ENSP00000494017.1:p.Ala387=
ENST00000265715.7:c.1161C>A ENSP00000265715.3:p.Ala387=
NM_000441.1:c.1161C>A NP_000432.1:p.Ala387=
XM_005250425.1:c.1161C>A XP_005250482.1:p.Ala387=
XM_006716025.2:c.1161C>A XP_006716088.1:p.Ala387=
XM_005250425.2:c.1161C>A XP_005250482.1:p.Ala387=
XM_006716025.3:c.1161C>A XP_006716088.1:p.Ala387=
XM_017012318.1:c.1161C>A XP_016867807.1:p.Ala387=
NM_000441.2:c.1161C>A MANE Select NP_000432.1:p.Ala387=
Search 100 bp 5'
Search 100 bp 3'