Canonical Allele Identifier: CA2415032250

Gene: GPR143

Linked Data

• dbSNP Id: rs2083523581

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765112_9765115dup , CM000685.2:g.9765112_9765115dup	GRCh38
NC_000023.10:g.9733152_9733155dup , CM000685.1:g.9733152_9733155dup	GRCh37
NC_000023.9:g.9693152_9693155dup	NCBI36
NG_009074.1:g.5763_5766dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+453_250+456dup MANE Select	ENSP00000417161.1:n.250+453_250+456dup
ENST00000431126.1:c.-3+1005_-3+1008dup	ENSP00000406138.1:n.-3+1005_-3+1008dup
ENST00000447366.5:c.-2-4289_-2-4286dup	ENSP00000390546.2:n.-2-4289_-2-4286dup
ENST00000467482.5:c.250+453_250+456dup	ENSP00000417161.1:n.250+453_250+456dup
NM_000273.2:c.250+453_250+456dup	NP_000264.2:n.250+453_250+456dup
XM_005274541.2:c.250+453_250+456dup	XP_005274598.1:n.250+453_250+456dup
XM_005274541.3:c.250+453_250+456dup	XP_005274598.1:n.250+453_250+456dup
XM_024452387.1:c.-2-4289_-2-4286dup	XP_024308155.1:n.-2-4289_-2-4286dup
XM_024452388.1:c.-2-4289_-2-4286dup	XP_024308156.1:n.-2-4289_-2-4286dup
NM_000273.3:c.250+453_250+456dup MANE Select	NP_000264.2:n.250+453_250+456dup