Canonical Allele Identifier: CA411322563

Gene: SLC5A4 SLC5A4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32239038A>G , CM000684.2:g.32239038A>G	GRCh38
NC_000022.10:g.32635025A>G , CM000684.1:g.32635025A>G	GRCh37
NC_000022.9:g.30965025A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266086.6:c.530T>C (SLC5A4) MANE Select	ENSP00000266086.3:p.Leu177Pro
ENST00000266086.5:c.530T>C (SLC5A4)	ENSP00000266086.3:p.Leu177Pro
NM_014227.2:c.530T>C (SLC5A4)	NP_055042.1:p.Leu177Pro
XM_006724308.2:c.392T>C (SLC5A4)	XP_006724371.1:p.Leu131Pro
XM_011530342.1:c.392T>C (SLC5A4)	XP_011528644.1:p.Leu131Pro
XM_011530343.1:c.392T>C (SLC5A4)	XP_011528645.1:p.Leu131Pro
XM_011530344.1:c.323T>C (SLC5A4)	XP_011528646.1:p.Leu108Pro
NR_149072.1:n.275-29250A>G (SLC5A4-AS1)
XM_006724308.3:c.392T>C (SLC5A4)	XP_006724371.1:p.Leu131Pro
XM_011530342.2:c.392T>C (SLC5A4)	XP_011528644.1:p.Leu131Pro
XM_011530343.2:c.392T>C (SLC5A4)	XP_011528645.1:p.Leu131Pro
XM_011530344.2:c.323T>C (SLC5A4)	XP_011528646.1:p.Leu108Pro
XM_017028920.1:c.620T>C (SLC5A4)	XP_016884409.1:p.Leu207Pro
NM_014227.3:c.530T>C (SLC5A4) MANE Select	NP_055042.1:p.Leu177Pro