Canonical Allele Identifier: CA2579547955
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741391_9741395del , CM000685.2:g.9741391_9741395del GRCh38
NC_000023.10:g.9709431_9709435del , CM000685.1:g.9709431_9709435del GRCh37
NC_000023.9:g.9669431_9669435del NCBI36
NG_009074.1:g.29483_29487del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.828_832del MANE Select ENSP00000417161.1:p.Ile276MetfsTer?
ENST00000447366.5:c.576_580del ENSP00000390546.2:p.Ile192MetfsTer?
ENST00000467482.5:c.828_832del ENSP00000417161.1:p.Ile276MetfsTer?
NM_000273.2:c.828_832del NP_000264.2:p.Ile276MetfsTer?
XM_005274541.2:c.828_832del XP_005274598.1:p.Ile276MetfsTer?
XM_005274541.3:c.828_832del XP_005274598.1:p.Ile276MetfsTer?
XM_024452387.1:c.576_580del XP_024308155.1:p.Ile192MetfsTer?
XM_024452388.1:c.576_580del XP_024308156.1:p.Ile192MetfsTer?
NM_000273.3:c.828_832del MANE Select NP_000264.2:p.Ile276MetfsTer?