Canonical Allele Identifier: CA457104682
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107710175-G-A
MyVariant Identifiers: chr7:g.107350620G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710175G>A , CM000669.2:g.107710175G>A GRCh38
NC_000007.13:g.107350620G>A , CM000669.1:g.107350620G>A GRCh37
NC_000007.12:g.107137856G>A NCBI36
NG_008489.1:g.54541G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2211G>A MANE Select ENSP00000494017.1:p.Glu737=
ENST00000644846.1:c.867G>A
ENST00000265715.7:c.2211G>A ENSP00000265715.3:p.Glu737=
ENST00000492030.2:n.397G>A
NM_000441.1:c.2211G>A NP_000432.1:p.Glu737=
XM_005250425.1:c.2211G>A XP_005250482.1:p.Glu737=
XM_005250425.2:c.2211G>A XP_005250482.1:p.Glu737=
XM_017012318.1:c.2133G>A XP_016867807.1:p.Glu711=
NM_000441.2:c.2211G>A MANE Select NP_000432.1:p.Glu737=
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