Canonical Allele Identifier: CA2527761373
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765265_9765352del , CM000685.2:g.9765265_9765352del GRCh38
NC_000023.10:g.9733305_9733392del , CM000685.1:g.9733305_9733392del GRCh37
NC_000023.9:g.9693305_9693392del NCBI36
NG_009074.1:g.5533_5620del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.250+223_250+310del MANE Select ENSP00000417161.1:n.250+223_250+310del
ENST00000431126.1:c.-3+775_-3+862del ENSP00000406138.1:n.-3+775_-3+862del
ENST00000447366.5:c.-2-4519_-2-4432del ENSP00000390546.2:n.-2-4519_-2-4432del
ENST00000467482.5:c.250+223_250+310del ENSP00000417161.1:n.250+223_250+310del
NM_000273.2:c.250+223_250+310del NP_000264.2:n.250+223_250+310del
XM_005274541.2:c.250+223_250+310del XP_005274598.1:n.250+223_250+310del
XM_005274541.3:c.250+223_250+310del XP_005274598.1:n.250+223_250+310del
XM_024452387.1:c.-2-4519_-2-4432del XP_024308155.1:n.-2-4519_-2-4432del
XM_024452388.1:c.-2-4519_-2-4432del XP_024308156.1:n.-2-4519_-2-4432del
NM_000273.3:c.250+223_250+310del MANE Select NP_000264.2:n.250+223_250+310del