Canonical Allele Identifier: CA261402
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43497
dbSNP Id: rs111033305

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107690200G>C , CM000669.2:g.107690200G>C GRCh38
NC_000007.13:g.107330645G>C , CM000669.1:g.107330645G>C GRCh37
NC_000007.12:g.107117881G>C NCBI36
NG_008489.1:g.34566G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1226G>C MANE Select ENSP00000494017.1:p.Arg409Pro
ENST00000265715.7:c.1226G>C ENSP00000265715.3:p.Arg409Pro
NM_000441.1:c.1226G>C NP_000432.1:p.Arg409Pro
XM_005250425.1:c.1226G>C XP_005250482.1:p.Arg409Pro
XM_006716025.2:c.1226G>C XP_006716088.1:p.Arg409Pro
XM_005250425.2:c.1226G>C XP_005250482.1:p.Arg409Pro
XM_006716025.3:c.1226G>C XP_006716088.1:p.Arg409Pro
XM_017012318.1:c.1226G>C XP_016867807.1:p.Arg409Pro
NM_000441.2:c.1226G>C MANE Select NP_000432.1:p.Arg409Pro