Canonical Allele Identifier: CA2415032287

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765181_9765182delinsTC , CM000685.2:g.9765181_9765182delinsTC	GRCh38
NC_000023.10:g.9733221_9733222delinsTC , CM000685.1:g.9733221_9733222delinsTC	GRCh37
NC_000023.9:g.9693221_9693222delinsTC	NCBI36
NG_009074.1:g.5696_5697delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+386_250+387delinsGA MANE Select	ENSP00000417161.1:n.250+386_250+387delinsGA
ENST00000431126.1:c.-3+938_-3+939delinsGA	ENSP00000406138.1:n.-3+938_-3+939delinsGA
ENST00000447366.5:c.-2-4356_-2-4355delinsGA	ENSP00000390546.2:n.-2-4356_-2-4355delinsGA
ENST00000467482.5:c.250+386_250+387delinsGA	ENSP00000417161.1:n.250+386_250+387delinsGA
NM_000273.2:c.250+386_250+387delinsGA	NP_000264.2:n.250+386_250+387delinsGA
XM_005274541.2:c.250+386_250+387delinsGA	XP_005274598.1:n.250+386_250+387delinsGA
XM_005274541.3:c.250+386_250+387delinsGA	XP_005274598.1:n.250+386_250+387delinsGA
XM_024452387.1:c.-2-4356_-2-4355delinsGA	XP_024308155.1:n.-2-4356_-2-4355delinsGA
XM_024452388.1:c.-2-4356_-2-4355delinsGA	XP_024308156.1:n.-2-4356_-2-4355delinsGA
NM_000273.3:c.250+386_250+387delinsGA MANE Select	NP_000264.2:n.250+386_250+387delinsGA