Canonical Allele Identifier: CA2819650374
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765434_9765521del , CM000685.2:g.9765434_9765521del GRCh38
NC_000023.10:g.9733474_9733561del , CM000685.1:g.9733474_9733561del GRCh37
NC_000023.9:g.9693474_9693561del NCBI36
NG_009074.1:g.5363_5450del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.250+53_250+140del MANE Select ENSP00000417161.1:n.250+53_250+140del
ENST00000431126.1:c.-3+605_-3+692del ENSP00000406138.1:n.-3+605_-3+692del
ENST00000447366.5:c.-2-4689_-2-4602del ENSP00000390546.2:n.-2-4689_-2-4602del
ENST00000467482.5:c.250+53_250+140del ENSP00000417161.1:n.250+53_250+140del
NM_000273.2:c.250+53_250+140del NP_000264.2:n.250+53_250+140del
XM_005274541.2:c.250+53_250+140del XP_005274598.1:n.250+53_250+140del
XM_005274541.3:c.250+53_250+140del XP_005274598.1:n.250+53_250+140del
XM_024452387.1:c.-2-4689_-2-4602del XP_024308155.1:n.-2-4689_-2-4602del
XM_024452388.1:c.-2-4689_-2-4602del XP_024308156.1:n.-2-4689_-2-4602del
NM_000273.3:c.250+53_250+140del MANE Select NP_000264.2:n.250+53_250+140del