Canonical Allele Identifier: CA2684457328
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107661924-G-GAGC
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107661924_107661925insAGC , CM000669.2:g.107661924_107661925insAGC GRCh38
NC_000007.13:g.107302369_107302370insAGC , CM000669.1:g.107302369_107302370insAGC GRCh37
NC_000007.12:g.107089605_107089606insAGC NCBI36
NG_008489.1:g.6290_6291insAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.164+119_164+120insAGC MANE Select ENSP00000494017.1:n.164+119_164+120insAGC
ENST00000265715.7:c.164+119_164+120insAGC ENSP00000265715.3:n.164+119_164+120insAGC
ENST00000440056.1:c.164+119_164+120insAGC ENSP00000394760.1:n.164+119_164+120insAGC
NM_000441.1:c.164+119_164+120insAGC NP_000432.1:n.164+119_164+120insAGC
XM_005250425.1:c.164+119_164+120insAGC XP_005250482.1:n.164+119_164+120insAGC
XM_006716025.2:c.164+119_164+120insAGC XP_006716088.1:n.164+119_164+120insAGC
XM_005250425.2:c.164+119_164+120insAGC XP_005250482.1:n.164+119_164+120insAGC
XM_006716025.3:c.164+119_164+120insAGC XP_006716088.1:n.164+119_164+120insAGC
XM_017012318.1:c.164+119_164+120insAGC XP_016867807.1:n.164+119_164+120insAGC
NM_000441.2:c.164+119_164+120insAGC MANE Select NP_000432.1:n.164+119_164+120insAGC
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