Canonical Allele Identifier: CA2819650370
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765346_9765347del , CM000685.2:g.9765346_9765347del GRCh38
NC_000023.10:g.9733386_9733387del , CM000685.1:g.9733386_9733387del GRCh37
NC_000023.9:g.9693386_9693387del NCBI36
NG_009074.1:g.5531_5532del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.250+221_250+222del MANE Select ENSP00000417161.1:n.250+221_250+222del
ENST00000431126.1:c.-3+773_-3+774del ENSP00000406138.1:n.-3+773_-3+774del
ENST00000447366.5:c.-2-4521_-2-4520del ENSP00000390546.2:n.-2-4521_-2-4520del
ENST00000467482.5:c.250+221_250+222del ENSP00000417161.1:n.250+221_250+222del
NM_000273.2:c.250+221_250+222del NP_000264.2:n.250+221_250+222del
XM_005274541.2:c.250+221_250+222del XP_005274598.1:n.250+221_250+222del
XM_005274541.3:c.250+221_250+222del XP_005274598.1:n.250+221_250+222del
XM_024452387.1:c.-2-4521_-2-4520del XP_024308155.1:n.-2-4521_-2-4520del
XM_024452388.1:c.-2-4521_-2-4520del XP_024308156.1:n.-2-4521_-2-4520del
NM_000273.3:c.250+221_250+222del MANE Select NP_000264.2:n.250+221_250+222del