Canonical Allele Identifier: CA2684466425
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107689309-A-AACCCAATAAGGTCTGGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689309_107689310insACCCAATAAGGTCTGGT , CM000669.2:g.107689309_107689310insACCCAATAAGGTCTGGT GRCh38
NC_000007.13:g.107329754_107329755insACCCAATAAGGTCTGGT , CM000669.1:g.107329754_107329755insACCCAATAAGGTCTGGT GRCh37
NC_000007.12:g.107116990_107116991insACCCAATAAGGTCTGGT NCBI36
NG_008489.1:g.33675_33676insACCCAATAAGGTCTGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+109_1149+110insACCCAATAAGGTCTGGT MANE Select ENSP00000494017.1:n.1149+109_1149+110insACCCAATAAGGTCTGGT
ENST00000265715.7:c.1149+109_1149+110insACCCAATAAGGTCTGGT ENSP00000265715.3:n.1149+109_1149+110insACCCAATAAGGTCTGGT
NM_000441.1:c.1149+109_1149+110insACCCAATAAGGTCTGGT NP_000432.1:n.1149+109_1149+110insACCCAATAAGGTCTGGT
XM_005250425.1:c.1149+109_1149+110insACCCAATAAGGTCTGGT XP_005250482.1:n.1149+109_1149+110insACCCAATAAGGTCTGGT
XM_006716025.2:c.1149+109_1149+110insACCCAATAAGGTCTGGT XP_006716088.1:n.1149+109_1149+110insACCCAATAAGGTCTGGT
XM_005250425.2:c.1149+109_1149+110insACCCAATAAGGTCTGGT XP_005250482.1:n.1149+109_1149+110insACCCAATAAGGTCTGGT
XM_006716025.3:c.1149+109_1149+110insACCCAATAAGGTCTGGT XP_006716088.1:n.1149+109_1149+110insACCCAATAAGGTCTGGT
XM_017012318.1:c.1149+109_1149+110insACCCAATAAGGTCTGGT XP_016867807.1:n.1149+109_1149+110insACCCAATAAGGTCTGGT
NM_000441.2:c.1149+109_1149+110insACCCAATAAGGTCTGGT MANE Select NP_000432.1:n.1149+109_1149+110insACCCAATAAGGTCTGGT
Search 100 bp 5'
Search 100 bp 3'