Canonical Allele Identifier: CA1732747577
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689395_107689396delinsGA , CM000669.2:g.107689395_107689396delinsGA GRCh38
NC_000007.13:g.107329840_107329841delinsGA , CM000669.1:g.107329840_107329841delinsGA GRCh37
NC_000007.12:g.107117076_107117077delinsGA NCBI36
NG_008489.1:g.33761_33762delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+195_1149+196delinsGA MANE Select ENSP00000494017.1:n.1149+195_1149+196delinsGA
ENST00000265715.7:c.1149+195_1149+196delinsGA ENSP00000265715.3:n.1149+195_1149+196delinsGA
NM_000441.1:c.1149+195_1149+196delinsGA NP_000432.1:n.1149+195_1149+196delinsGA
XM_005250425.1:c.1149+195_1149+196delinsGA XP_005250482.1:n.1149+195_1149+196delinsGA
XM_006716025.2:c.1149+195_1149+196delinsGA XP_006716088.1:n.1149+195_1149+196delinsGA
XM_005250425.2:c.1149+195_1149+196delinsGA XP_005250482.1:n.1149+195_1149+196delinsGA
XM_006716025.3:c.1149+195_1149+196delinsGA XP_006716088.1:n.1149+195_1149+196delinsGA
XM_017012318.1:c.1149+195_1149+196delinsGA XP_016867807.1:n.1149+195_1149+196delinsGA
NM_000441.2:c.1149+195_1149+196delinsGA MANE Select NP_000432.1:n.1149+195_1149+196delinsGA
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