Canonical Allele Identifier: CA2578989113
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710254_107710255del , CM000669.2:g.107710254_107710255del GRCh38
NC_000007.13:g.107350699_107350700del , CM000669.1:g.107350699_107350700del GRCh37
NC_000007.12:g.107137935_107137936del NCBI36
NG_008489.1:g.54620_54621del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2235+55_2235+56del MANE Select ENSP00000494017.1:n.2235+55_2235+56del
ENST00000644846.1:c.891+55_891+56del
ENST00000265715.7:c.2235+55_2235+56del ENSP00000265715.3:n.2235+55_2235+56del
ENST00000492030.2:n.421+55_421+56del
NM_000441.1:c.2235+55_2235+56del NP_000432.1:n.2235+55_2235+56del
XM_005250425.1:c.2235+55_2235+56del XP_005250482.1:n.2235+55_2235+56del
XM_005250425.2:c.2235+55_2235+56del XP_005250482.1:n.2235+55_2235+56del
XM_017012318.1:c.2157+55_2157+56del XP_016867807.1:n.2157+55_2157+56del
NM_000441.2:c.2235+55_2235+56del MANE Select NP_000432.1:n.2235+55_2235+56del