Canonical Allele Identifier: CA1732747208
Gene: SLC26A4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107675163T= , CM000669.2:g.107675163T= GRCh38
NC_000007.13:g.107315608T= , CM000669.1:g.107315608T= GRCh37
NC_000007.12:g.107102844T= NCBI36
NG_008489.1:g.19529T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.765+54T= MANE Select ENSP00000494017.1:n.765+54T=
ENST00000265715.7:c.765+54T= ENSP00000265715.3:n.765+54T=
NM_000441.1:c.765+54T= NP_000432.1:n.765+54T=
XM_005250425.1:c.765+54T= XP_005250482.1:n.765+54T=
XM_006716025.2:c.765+54T= XP_006716088.1:n.765+54T=
XM_005250425.2:c.765+54T= XP_005250482.1:n.765+54T=
XM_006716025.3:c.765+54T= XP_006716088.1:n.765+54T=
XM_017012318.1:c.765+54T= XP_016867807.1:n.765+54T=
NM_000441.2:c.765+54T= MANE Select NP_000432.1:n.765+54T=
Search 100 bp 5'
Search 100 bp 3'