Canonical Allele Identifier: CA2415030058
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9759332C= , CM000685.2:g.9759332C= GRCh38
NC_000023.10:g.9727372C= , CM000685.1:g.9727372C= GRCh37
NC_000023.9:g.9687372C= NCBI36
NG_009074.1:g.11546G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.455G= MANE Select ENSP00000417161.1:p.Ser152=
ENST00000431126.1:c.203G= ENSP00000406138.1:p.Ser68=
ENST00000447366.5:c.203G= ENSP00000390546.2:p.Ser68=
ENST00000467482.5:c.455G= ENSP00000417161.1:p.Ser152=
ENST00000480178.1:n.63G=
NM_000273.2:c.455G= NP_000264.2:p.Ser152=
XM_005274541.2:c.455G= XP_005274598.1:p.Ser152=
XM_005274541.3:c.455G= XP_005274598.1:p.Ser152=
XM_024452387.1:c.203G= XP_024308155.1:p.Ser68=
XM_024452388.1:c.203G= XP_024308156.1:p.Ser68=
NM_000273.3:c.455G= MANE Select NP_000264.2:p.Ser152=