Canonical Allele Identifier: CA1732751438
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710232T= , CM000669.2:g.107710232T= GRCh38
NC_000007.13:g.107350677T= , CM000669.1:g.107350677T= GRCh37
NC_000007.12:g.107137913T= NCBI36
NG_008489.1:g.54598T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2235+33T= MANE Select ENSP00000494017.1:n.2235+33T=
ENST00000644846.1:c.891+33T=
ENST00000265715.7:c.2235+33T= ENSP00000265715.3:n.2235+33T=
ENST00000492030.2:n.421+33T=
NM_000441.1:c.2235+33T= NP_000432.1:n.2235+33T=
XM_005250425.1:c.2235+33T= XP_005250482.1:n.2235+33T=
XM_005250425.2:c.2235+33T= XP_005250482.1:n.2235+33T=
XM_017012318.1:c.2157+33T= XP_016867807.1:n.2157+33T=
NM_000441.2:c.2235+33T= MANE Select NP_000432.1:n.2235+33T=