Canonical Allele Identifier: CA1732752990
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695884G= , CM000669.2:g.107695884G= GRCh38
NC_000007.13:g.107336329G= , CM000669.1:g.107336329G= GRCh37
NC_000007.12:g.107123565G= NCBI36
NG_008489.1:g.40250G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1438-49G= MANE Select ENSP00000494017.1:n.1438-49G=
ENST00000644846.1:c.149-49G=
ENST00000265715.7:c.1438-49G= ENSP00000265715.3:n.1438-49G=
ENST00000460748.1:n.541-49G=
ENST00000477350.5:n.285-49G=
ENST00000480841.5:n.287-49G=
ENST00000497446.5:n.453-49G=
NM_000441.1:c.1438-49G= NP_000432.1:n.1438-49G=
XM_005250425.1:c.1438-49G= XP_005250482.1:n.1438-49G=
XM_005250425.2:c.1438-49G= XP_005250482.1:n.1438-49G=
XM_017012318.1:c.1360-49G= XP_016867807.1:n.1360-49G=
NM_000441.2:c.1438-49G= MANE Select NP_000432.1:n.1438-49G=