Canonical Allele Identifier: CA1732747435
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689236G= , CM000669.2:g.107689236G= GRCh38
NC_000007.13:g.107329681G= , CM000669.1:g.107329681G= GRCh37
NC_000007.12:g.107116917G= NCBI36
NG_008489.1:g.33602G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+36G= MANE Select ENSP00000494017.1:n.1149+36G=
ENST00000265715.7:c.1149+36G= ENSP00000265715.3:n.1149+36G=
NM_000441.1:c.1149+36G= NP_000432.1:n.1149+36G=
XM_005250425.1:c.1149+36G= XP_005250482.1:n.1149+36G=
XM_006716025.2:c.1149+36G= XP_006716088.1:n.1149+36G=
XM_005250425.2:c.1149+36G= XP_005250482.1:n.1149+36G=
XM_006716025.3:c.1149+36G= XP_006716088.1:n.1149+36G=
XM_017012318.1:c.1149+36G= XP_016867807.1:n.1149+36G=
NM_000441.2:c.1149+36G= MANE Select NP_000432.1:n.1149+36G=