Canonical Allele Identifier: CA2326080533
Community Standard Title: NM_000453.3(SLC5A5):c.1628G= (p.Gly543=)
Gene: SLC5A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17888432G= , CM000681.2:g.17888432G= GRCh38
NC_000019.9:g.17999241G= , CM000681.1:g.17999241G= GRCh37
NC_000019.8:g.17860241G= NCBI36
NG_012930.1:g.21460G=

Transcript Alleles

HGVS Amino-acid Change
NM_000453.3:c.1628G= MANE Select NP_000444.1:p.Gly543=
ENST00000222248.4:c.1628G= MANE Select ENSP00000222248.2:p.Gly543=
NM_000453.2:c.1628G= NP_000444.1:p.Gly543=
ENST00000222248.3:c.1628G= ENSP00000222248.2:p.Gly543=
XM_011528192.1:c.1661G= XP_011526494.1:p.Gly554=
XM_011528192.2:c.1661G= XP_011526494.1:p.Gly554=
XM_011528193.1:c.1394G= XP_011526495.1:p.Gly465=
XM_011528193.3:c.1394G= XP_011526495.1:p.Gly465=
XM_011528194.1:c.1295G= XP_011526496.1:p.Gly432=
XM_011528194.3:c.1295G= XP_011526496.1:p.Gly432=
XM_017027158.1:c.1361G= XP_016882647.1:p.Gly454=