Canonical Allele Identifier: CA1130984015

Gene: GPR143

Linked Data

• dbSNP Id: rs2083523195

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765046_9765064del , CM000685.2:g.9765046_9765064del	GRCh38
NC_000023.10:g.9733086_9733104del , CM000685.1:g.9733086_9733104del	GRCh37
NC_000023.9:g.9693086_9693104del	NCBI36
NG_009074.1:g.5816_5834del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+506_250+524del MANE Select	ENSP00000417161.1:n.250+506_250+524del
ENST00000431126.1:c.-3+1058_-3+1076del	ENSP00000406138.1:n.-3+1058_-3+1076del
ENST00000447366.5:c.-2-4236_-2-4218del	ENSP00000390546.2:n.-2-4236_-2-4218del
ENST00000467482.5:c.250+506_250+524del	ENSP00000417161.1:n.250+506_250+524del
NM_000273.2:c.250+506_250+524del	NP_000264.2:n.250+506_250+524del
XM_005274541.2:c.250+506_250+524del	XP_005274598.1:n.250+506_250+524del
XM_005274541.3:c.250+506_250+524del	XP_005274598.1:n.250+506_250+524del
XM_024452387.1:c.-2-4236_-2-4218del	XP_024308155.1:n.-2-4236_-2-4218del
XM_024452388.1:c.-2-4236_-2-4218del	XP_024308156.1:n.-2-4236_-2-4218del
NM_000273.3:c.250+506_250+524del MANE Select	NP_000264.2:n.250+506_250+524del