Canonical Allele Identifier: CA10199615
Gene: SLC5A4 HGNC NCBI
SLC5A4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32239032A>G , CM000684.2:g.32239032A>G GRCh38
NC_000022.10:g.32635019A>G , CM000684.1:g.32635019A>G GRCh37
NC_000022.9:g.30965019A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266086.6:c.536T>C (SLC5A4) MANE Select ENSP00000266086.3:p.Leu179Pro
ENST00000266086.5:c.536T>C (SLC5A4) ENSP00000266086.3:p.Leu179Pro
NM_014227.2:c.536T>C (SLC5A4) NP_055042.1:p.Leu179Pro
XM_006724308.2:c.398T>C (SLC5A4) XP_006724371.1:p.Leu133Pro
XM_011530342.1:c.398T>C (SLC5A4) XP_011528644.1:p.Leu133Pro
XM_011530343.1:c.398T>C (SLC5A4) XP_011528645.1:p.Leu133Pro
XM_011530344.1:c.329T>C (SLC5A4) XP_011528646.1:p.Leu110Pro
NR_149072.1:n.275-29256A>G (SLC5A4-AS1)
XM_006724308.3:c.398T>C (SLC5A4) XP_006724371.1:p.Leu133Pro
XM_011530342.2:c.398T>C (SLC5A4) XP_011528644.1:p.Leu133Pro
XM_011530343.2:c.398T>C (SLC5A4) XP_011528645.1:p.Leu133Pro
XM_011530344.2:c.329T>C (SLC5A4) XP_011528646.1:p.Leu110Pro
XM_017028920.1:c.626T>C (SLC5A4) XP_016884409.1:p.Leu209Pro
NM_014227.3:c.536T>C (SLC5A4) MANE Select NP_055042.1:p.Leu179Pro