Canonical Allele Identifier: CA2529994702
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710267_107710268insGT , CM000669.2:g.107710267_107710268insGT GRCh38
NC_000007.13:g.107350712_107350713insGT , CM000669.1:g.107350712_107350713insGT GRCh37
NC_000007.12:g.107137948_107137949insGT NCBI36
NG_008489.1:g.54633_54634insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2235+68_2235+69insGT MANE Select ENSP00000494017.1:n.2235+68_2235+69insGT
ENST00000644846.1:c.891+68_891+69insGT
ENST00000265715.7:c.2235+68_2235+69insGT ENSP00000265715.3:n.2235+68_2235+69insGT
ENST00000492030.2:n.421+68_421+69insGT
NM_000441.1:c.2235+68_2235+69insGT NP_000432.1:n.2235+68_2235+69insGT
XM_005250425.1:c.2235+68_2235+69insGT XP_005250482.1:n.2235+68_2235+69insGT
XM_005250425.2:c.2235+68_2235+69insGT XP_005250482.1:n.2235+68_2235+69insGT
XM_017012318.1:c.2157+68_2157+69insGT XP_016867807.1:n.2157+68_2157+69insGT
NM_000441.2:c.2235+68_2235+69insGT MANE Select NP_000432.1:n.2235+68_2235+69insGT