Canonical Allele Identifier: CA1732747485
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689316_107689317delinsAT , CM000669.2:g.107689316_107689317delinsAT GRCh38
NC_000007.13:g.107329761_107329762delinsAT , CM000669.1:g.107329761_107329762delinsAT GRCh37
NC_000007.12:g.107116997_107116998delinsAT NCBI36
NG_008489.1:g.33682_33683delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+116_1149+117delinsAT MANE Select ENSP00000494017.1:n.1149+116_1149+117delinsAT
ENST00000265715.7:c.1149+116_1149+117delinsAT ENSP00000265715.3:n.1149+116_1149+117delinsAT
NM_000441.1:c.1149+116_1149+117delinsAT NP_000432.1:n.1149+116_1149+117delinsAT
XM_005250425.1:c.1149+116_1149+117delinsAT XP_005250482.1:n.1149+116_1149+117delinsAT
XM_006716025.2:c.1149+116_1149+117delinsAT XP_006716088.1:n.1149+116_1149+117delinsAT
XM_005250425.2:c.1149+116_1149+117delinsAT XP_005250482.1:n.1149+116_1149+117delinsAT
XM_006716025.3:c.1149+116_1149+117delinsAT XP_006716088.1:n.1149+116_1149+117delinsAT
XM_017012318.1:c.1149+116_1149+117delinsAT XP_016867807.1:n.1149+116_1149+117delinsAT
NM_000441.2:c.1149+116_1149+117delinsAT MANE Select NP_000432.1:n.1149+116_1149+117delinsAT