Canonical Allele Identifier: CA2415032503
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765624_9765653delinsGGCGGGGACGTCGCGGGGGACCCGGGGCCC , CM000685.2:g.9765624_9765653delinsGGCGGGGACGTCGCGGGGGACCCGGGGCCC GRCh38
NC_000023.10:g.9733664_9733693delinsGGCGGGGACGTCGCGGGGGACCCGGGGCCC , CM000685.1:g.9733664_9733693delinsGGCGGGGACGTCGCGGGGGACCCGGGGCCC GRCh37
NC_000023.9:g.9693664_9693693delinsGGCGGGGACGTCGCGGGGGACCCGGGGCCC NCBI36
NG_009074.1:g.5225_5254delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.165_194delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC MANE Select ENSP00000417161.1:p.Ala55=
ENST00000431126.1:c.-3+467_-3+496delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC ENSP00000406138.1:n.-3+467_-3+496delinsGG...
ENST00000447366.5:c.-2-4827_-2-4798delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC ENSP00000390546.2:n.-2-4827_-2-4798delins...
ENST00000467482.5:c.165_194delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC ENSP00000417161.1:p.Ala55=
NM_000273.2:c.165_194delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC NP_000264.2:p.Ala55=
XM_005274541.2:c.165_194delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC XP_005274598.1:p.Ala55=
XM_005274541.3:c.165_194delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC XP_005274598.1:p.Ala55=
XM_024452387.1:c.-2-4827_-2-4798delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC XP_024308155.1:n.-2-4827_-2-4798delinsGGG...
XM_024452388.1:c.-2-4827_-2-4798delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC XP_024308156.1:n.-2-4827_-2-4798delinsGGG...
NM_000273.3:c.165_194delinsGGGCCCCGGGTCCCCCGCGACGTCCCCGCC MANE Select NP_000264.2:p.Ala55=