Canonical Allele Identifier: CA2684468728
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710215_107710216del , CM000669.2:g.107710215_107710216del GRCh38
NC_000007.13:g.107350660_107350661del , CM000669.1:g.107350660_107350661del GRCh37
NC_000007.12:g.107137896_107137897del NCBI36
NG_008489.1:g.54581_54582del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2235+16_2235+17del MANE Select ENSP00000494017.1:n.2235+16_2235+17del
ENST00000644846.1:c.891+16_891+17del
ENST00000265715.7:c.2235+16_2235+17del ENSP00000265715.3:n.2235+16_2235+17del
ENST00000492030.2:n.421+16_421+17del
NM_000441.1:c.2235+16_2235+17del NP_000432.1:n.2235+16_2235+17del
XM_005250425.1:c.2235+16_2235+17del XP_005250482.1:n.2235+16_2235+17del
XM_005250425.2:c.2235+16_2235+17del XP_005250482.1:n.2235+16_2235+17del
XM_017012318.1:c.2157+16_2157+17del XP_016867807.1:n.2157+16_2157+17del
NM_000441.2:c.2235+16_2235+17del MANE Select NP_000432.1:n.2235+16_2235+17del