Canonical Allele Identifier: CA2819650357
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765206_9765249del , CM000685.2:g.9765206_9765249del GRCh38
NC_000023.10:g.9733246_9733289del , CM000685.1:g.9733246_9733289del GRCh37
NC_000023.9:g.9693246_9693289del NCBI36
NG_009074.1:g.5631_5674del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.250+321_250+364del MANE Select ENSP00000417161.1:n.250+321_250+364del
ENST00000431126.1:c.-3+873_-3+916del ENSP00000406138.1:n.-3+873_-3+916del
ENST00000447366.5:c.-2-4421_-2-4378del ENSP00000390546.2:n.-2-4421_-2-4378del
ENST00000467482.5:c.250+321_250+364del ENSP00000417161.1:n.250+321_250+364del
NM_000273.2:c.250+321_250+364del NP_000264.2:n.250+321_250+364del
XM_005274541.2:c.250+321_250+364del XP_005274598.1:n.250+321_250+364del
XM_005274541.3:c.250+321_250+364del XP_005274598.1:n.250+321_250+364del
XM_024452387.1:c.-2-4421_-2-4378del XP_024308155.1:n.-2-4421_-2-4378del
XM_024452388.1:c.-2-4421_-2-4378del XP_024308156.1:n.-2-4421_-2-4378del
NM_000273.3:c.250+321_250+364del MANE Select NP_000264.2:n.250+321_250+364del