Canonical Allele Identifier: CA1105638844
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107690370_107690371insGGGGACA , CM000669.2:g.107690370_107690371insGGGGACA GRCh38
NC_000007.13:g.107330815_107330816insGGGGACA , CM000669.1:g.107330815_107330816insGGGGACA GRCh37
NC_000007.12:g.107118051_107118052insGGGGACA NCBI36
NG_008489.1:g.34736_34737insGGGGACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1263+133_1263+134insGGGGACA MANE Select ENSP00000494017.1:n.1263+133_1263+134insGGGGACA
ENST00000265715.7:c.1263+133_1263+134insGGGGACA ENSP00000265715.3:n.1263+133_1263+134insGGGGACA
NM_000441.1:c.1263+133_1263+134insGGGGACA NP_000432.1:n.1263+133_1263+134insGGGGACA
XM_005250425.1:c.1263+133_1263+134insGGGGACA XP_005250482.1:n.1263+133_1263+134insGGGGACA
XM_006716025.2:c.1263+133_1263+134insGGGGACA XP_006716088.1:n.1263+133_1263+134insGGGGACA
XM_005250425.2:c.1263+133_1263+134insGGGGACA XP_005250482.1:n.1263+133_1263+134insGGGGACA
XM_006716025.3:c.1263+133_1263+134insGGGGACA XP_006716088.1:n.1263+133_1263+134insGGGGACA
XM_017012318.1:c.1263+133_1263+134insGGGGACA XP_016867807.1:n.1263+133_1263+134insGGGGACA
NM_000441.2:c.1263+133_1263+134insGGGGACA MANE Select NP_000432.1:n.1263+133_1263+134insGGGGACA