Canonical Allele Identifier: CA1732747382
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1791500894

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689151del , CM000669.2:g.107689151del GRCh38
NC_000007.13:g.107329596del , CM000669.1:g.107329596del GRCh37
NC_000007.12:g.107116832del NCBI36
NG_008489.1:g.33517del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1100del MANE Select ENSP00000494017.1:p.Val367GlufsTer?
ENST00000265715.7:c.1100del ENSP00000265715.3:p.Val367GlufsTer?
NM_000441.1:c.1100del NP_000432.1:p.Val367GlufsTer?
XM_005250425.1:c.1100del XP_005250482.1:p.Val367GlufsTer?
XM_006716025.2:c.1100del XP_006716088.1:p.Val367GlufsTer?
XM_005250425.2:c.1100del XP_005250482.1:p.Val367GlufsTer?
XM_006716025.3:c.1100del XP_006716088.1:p.Val367GlufsTer?
XM_017012318.1:c.1100del XP_016867807.1:p.Val367GlufsTer?
NM_000441.2:c.1100del MANE Select NP_000432.1:p.Val367GlufsTer?