Canonical Allele Identifier: CA2415024367
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741193G= , CM000685.2:g.9741193G= GRCh38
NC_000023.10:g.9709233G= , CM000685.1:g.9709233G= GRCh37
NC_000023.9:g.9669233G= NCBI36
NG_009074.1:g.29685C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+145C= MANE Select ENSP00000417161.1:n.885+145C=
ENST00000447366.5:c.633+145C= ENSP00000390546.2:n.633+145C=
ENST00000467482.5:c.885+145C= ENSP00000417161.1:n.885+145C=
NM_000273.2:c.885+145C= NP_000264.2:n.885+145C=
XM_005274541.2:c.885+145C= XP_005274598.1:n.885+145C=
XM_005274541.3:c.885+145C= XP_005274598.1:n.885+145C=
XM_024452387.1:c.633+145C= XP_024308155.1:n.633+145C=
XM_024452388.1:c.633+145C= XP_024308156.1:n.633+145C=
NM_000273.3:c.885+145C= MANE Select NP_000264.2:n.885+145C=