Canonical Allele Identifier: CA1732747533
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689365_107689366delinsTA , CM000669.2:g.107689365_107689366delinsTA GRCh38
NC_000007.13:g.107329810_107329811delinsTA , CM000669.1:g.107329810_107329811delinsTA GRCh37
NC_000007.12:g.107117046_107117047delinsTA NCBI36
NG_008489.1:g.33731_33732delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+165_1149+166delinsTA MANE Select ENSP00000494017.1:n.1149+165_1149+166delinsTA
ENST00000265715.7:c.1149+165_1149+166delinsTA ENSP00000265715.3:n.1149+165_1149+166delinsTA
NM_000441.1:c.1149+165_1149+166delinsTA NP_000432.1:n.1149+165_1149+166delinsTA
XM_005250425.1:c.1149+165_1149+166delinsTA XP_005250482.1:n.1149+165_1149+166delinsTA
XM_006716025.2:c.1149+165_1149+166delinsTA XP_006716088.1:n.1149+165_1149+166delinsTA
XM_005250425.2:c.1149+165_1149+166delinsTA XP_005250482.1:n.1149+165_1149+166delinsTA
XM_006716025.3:c.1149+165_1149+166delinsTA XP_006716088.1:n.1149+165_1149+166delinsTA
XM_017012318.1:c.1149+165_1149+166delinsTA XP_016867807.1:n.1149+165_1149+166delinsTA
NM_000441.2:c.1149+165_1149+166delinsTA MANE Select NP_000432.1:n.1149+165_1149+166delinsTA