Canonical Allele Identifier: CA2684466412
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689297del , CM000669.2:g.107689297del GRCh38
NC_000007.13:g.107329742del , CM000669.1:g.107329742del GRCh37
NC_000007.12:g.107116978del NCBI36
NG_008489.1:g.33663del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+97del MANE Select ENSP00000494017.1:n.1149+97del
ENST00000265715.7:c.1149+97del ENSP00000265715.3:n.1149+97del
NM_000441.1:c.1149+97del NP_000432.1:n.1149+97del
XM_005250425.1:c.1149+97del XP_005250482.1:n.1149+97del
XM_006716025.2:c.1149+97del XP_006716088.1:n.1149+97del
XM_005250425.2:c.1149+97del XP_005250482.1:n.1149+97del
XM_006716025.3:c.1149+97del XP_006716088.1:n.1149+97del
XM_017012318.1:c.1149+97del XP_016867807.1:n.1149+97del
NM_000441.2:c.1149+97del MANE Select NP_000432.1:n.1149+97del