Canonical Allele Identifier: CA2684468721
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710204dup , CM000669.2:g.107710204dup GRCh38
NC_000007.13:g.107350649dup , CM000669.1:g.107350649dup GRCh37
NC_000007.12:g.107137885dup NCBI36
NG_008489.1:g.54570dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2235+5dup MANE Select ENSP00000494017.1:n.2235+5dup
ENST00000644846.1:c.891+5dup
ENST00000265715.7:c.2235+5dup ENSP00000265715.3:n.2235+5dup
ENST00000492030.2:n.421+5dup
NM_000441.1:c.2235+5dup NP_000432.1:n.2235+5dup
XM_005250425.1:c.2235+5dup XP_005250482.1:n.2235+5dup
XM_005250425.2:c.2235+5dup XP_005250482.1:n.2235+5dup
XM_017012318.1:c.2157+5dup XP_016867807.1:n.2157+5dup
NM_000441.2:c.2235+5dup MANE Select NP_000432.1:n.2235+5dup