Canonical Allele Identifier: CA2579548192
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765614del , CM000685.2:g.9765614del GRCh38
NC_000023.10:g.9733654del , CM000685.1:g.9733654del GRCh37
NC_000023.9:g.9693654del NCBI36
NG_009074.1:g.5265del

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.205del MANE Select ENSP00000417161.1:p.Arg69AlafsTer18
ENST00000431126.1:c.-3+507del ENSP00000406138.1:n.-3+507del
ENST00000447366.5:c.-2-4787del ENSP00000390546.2:n.-2-4787del
ENST00000467482.5:c.205del ENSP00000417161.1:p.Arg69AlafsTer18
NM_000273.2:c.205del NP_000264.2:p.Arg69AlafsTer18
XM_005274541.2:c.205del XP_005274598.1:p.Arg69AlafsTer18
XM_005274541.3:c.205del XP_005274598.1:p.Arg69AlafsTer18
XM_024452387.1:c.-2-4787del XP_024308155.1:n.-2-4787del
XM_024452388.1:c.-2-4787del XP_024308156.1:n.-2-4787del
NM_000273.3:c.205del MANE Select NP_000264.2:p.Arg69AlafsTer18