Canonical Allele Identifier: CA2684457336
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107661926-T-TCTGG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107661926_107661927insCTGG , CM000669.2:g.107661926_107661927insCTGG GRCh38
NC_000007.13:g.107302371_107302372insCTGG , CM000669.1:g.107302371_107302372insCTGG GRCh37
NC_000007.12:g.107089607_107089608insCTGG NCBI36
NG_008489.1:g.6292_6293insCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.164+121_164+122insCTGG MANE Select ENSP00000494017.1:n.164+121_164+122insCTGG
ENST00000265715.7:c.164+121_164+122insCTGG ENSP00000265715.3:n.164+121_164+122insCTGG
ENST00000440056.1:c.164+121_164+122insCTGG ENSP00000394760.1:n.164+121_164+122insCTGG
NM_000441.1:c.164+121_164+122insCTGG NP_000432.1:n.164+121_164+122insCTGG
XM_005250425.1:c.164+121_164+122insCTGG XP_005250482.1:n.164+121_164+122insCTGG
XM_006716025.2:c.164+121_164+122insCTGG XP_006716088.1:n.164+121_164+122insCTGG
XM_005250425.2:c.164+121_164+122insCTGG XP_005250482.1:n.164+121_164+122insCTGG
XM_006716025.3:c.164+121_164+122insCTGG XP_006716088.1:n.164+121_164+122insCTGG
XM_017012318.1:c.164+121_164+122insCTGG XP_016867807.1:n.164+121_164+122insCTGG
NM_000441.2:c.164+121_164+122insCTGG MANE Select NP_000432.1:n.164+121_164+122insCTGG
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