Canonical Allele Identifier: CA411316261
Gene: SLC5A4 HGNC NCBI
SLC5A4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32218591A>G , CM000684.2:g.32218591A>G GRCh38
NC_000022.10:g.32614578A>G , CM000684.1:g.32614578A>G GRCh37
NC_000022.9:g.30944578A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266086.6:c.1903T>C (SLC5A4) MANE Select ENSP00000266086.3:p.Ser635Pro
ENST00000266086.5:c.1903T>C (SLC5A4) ENSP00000266086.3:p.Ser635Pro
NM_014227.2:c.1903T>C (SLC5A4) NP_055042.1:p.Ser635Pro
XM_006724308.2:c.1765T>C (SLC5A4) XP_006724371.1:p.Ser589Pro
XM_011530342.1:c.1765T>C (SLC5A4) XP_011528644.1:p.Ser589Pro
XM_011530343.1:c.1765T>C (SLC5A4) XP_011528645.1:p.Ser589Pro
XM_011530344.1:c.1696T>C (SLC5A4) XP_011528646.1:p.Ser566Pro
NR_149072.1:n.274+11315A>G (SLC5A4-AS1)
XM_006724308.3:c.1765T>C (SLC5A4) XP_006724371.1:p.Ser589Pro
XM_011530342.2:c.1765T>C (SLC5A4) XP_011528644.1:p.Ser589Pro
XM_011530343.2:c.1765T>C (SLC5A4) XP_011528645.1:p.Ser589Pro
XM_011530344.2:c.1696T>C (SLC5A4) XP_011528646.1:p.Ser566Pro
XM_017028920.1:c.1993T>C (SLC5A4) XP_016884409.1:p.Ser665Pro
NM_014227.3:c.1903T>C (SLC5A4) MANE Select NP_055042.1:p.Ser635Pro