Canonical Allele Identifier: CA2819650372
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765414_9765501del , CM000685.2:g.9765414_9765501del GRCh38
NC_000023.10:g.9733454_9733541del , CM000685.1:g.9733454_9733541del GRCh37
NC_000023.9:g.9693454_9693541del NCBI36
NG_009074.1:g.5382_5469del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.250+72_250+159del MANE Select ENSP00000417161.1:n.250+72_250+159del
ENST00000431126.1:c.-3+624_-3+711del ENSP00000406138.1:n.-3+624_-3+711del
ENST00000447366.5:c.-2-4670_-2-4583del ENSP00000390546.2:n.-2-4670_-2-4583del
ENST00000467482.5:c.250+72_250+159del ENSP00000417161.1:n.250+72_250+159del
NM_000273.2:c.250+72_250+159del NP_000264.2:n.250+72_250+159del
XM_005274541.2:c.250+72_250+159del XP_005274598.1:n.250+72_250+159del
XM_005274541.3:c.250+72_250+159del XP_005274598.1:n.250+72_250+159del
XM_024452387.1:c.-2-4670_-2-4583del XP_024308155.1:n.-2-4670_-2-4583del
XM_024452388.1:c.-2-4670_-2-4583del XP_024308156.1:n.-2-4670_-2-4583del
NM_000273.3:c.250+72_250+159del MANE Select NP_000264.2:n.250+72_250+159del