Canonical Allele Identifier: CA1732752727
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695670T= , CM000669.2:g.107695670T= GRCh38
NC_000007.13:g.107336115T= , CM000669.1:g.107336115T= GRCh37
NC_000007.12:g.107123351T= NCBI36
NG_008489.1:g.40036T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1438-263T= MANE Select ENSP00000494017.1:n.1438-263T=
ENST00000644846.1:c.149-263T=
ENST00000265715.7:c.1438-263T= ENSP00000265715.3:n.1438-263T=
ENST00000460748.1:n.541-263T=
ENST00000477350.5:n.285-263T=
ENST00000480841.5:n.287-263T=
ENST00000497446.5:n.453-263T=
NM_000441.1:c.1438-263T= NP_000432.1:n.1438-263T=
XM_005250425.1:c.1438-263T= XP_005250482.1:n.1438-263T=
XM_005250425.2:c.1438-263T= XP_005250482.1:n.1438-263T=
XM_017012318.1:c.1360-263T= XP_016867807.1:n.1360-263T=
NM_000441.2:c.1438-263T= MANE Select NP_000432.1:n.1438-263T=
Search 100 bp 5'
Search 100 bp 3'