Canonical Allele Identifier: CA1732751434
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710223A= , CM000669.2:g.107710223A= GRCh38
NC_000007.13:g.107350668A= , CM000669.1:g.107350668A= GRCh37
NC_000007.12:g.107137904A= NCBI36
NG_008489.1:g.54589A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2235+24A= MANE Select ENSP00000494017.1:n.2235+24A=
ENST00000644846.1:c.891+24A=
ENST00000265715.7:c.2235+24A= ENSP00000265715.3:n.2235+24A=
ENST00000492030.2:n.421+24A=
NM_000441.1:c.2235+24A= NP_000432.1:n.2235+24A=
XM_005250425.1:c.2235+24A= XP_005250482.1:n.2235+24A=
XM_005250425.2:c.2235+24A= XP_005250482.1:n.2235+24A=
XM_017012318.1:c.2157+24A= XP_016867807.1:n.2157+24A=
NM_000441.2:c.2235+24A= MANE Select NP_000432.1:n.2235+24A=