Canonical Allele Identifier: CA2563355279
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741323del , CM000685.2:g.9741323del GRCh38
NC_000023.10:g.9709363del , CM000685.1:g.9709363del GRCh37
NC_000023.9:g.9669363del NCBI36
NG_009074.1:g.29555del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+15del MANE Select ENSP00000417161.1:n.885+15del
ENST00000447366.5:c.633+15del ENSP00000390546.2:n.633+15del
ENST00000467482.5:c.885+15del ENSP00000417161.1:n.885+15del
NM_000273.2:c.885+15del NP_000264.2:n.885+15del
XM_005274541.2:c.885+15del XP_005274598.1:n.885+15del
XM_005274541.3:c.885+15del XP_005274598.1:n.885+15del
XM_024452387.1:c.633+15del XP_024308155.1:n.633+15del
XM_024452388.1:c.633+15del XP_024308156.1:n.633+15del
NM_000273.3:c.885+15del MANE Select NP_000264.2:n.885+15del