Canonical Allele Identifier: CA2560101186

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765219_9765262del , CM000685.2:g.9765219_9765262del	GRCh38
NC_000023.10:g.9733259_9733302del , CM000685.1:g.9733259_9733302del	GRCh37
NC_000023.9:g.9693259_9693302del	NCBI36
NG_009074.1:g.5626_5669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+316_250+359del MANE Select	ENSP00000417161.1:n.250+316_250+359del
ENST00000431126.1:c.-3+868_-3+911del	ENSP00000406138.1:n.-3+868_-3+911del
ENST00000447366.5:c.-2-4426_-2-4383del	ENSP00000390546.2:n.-2-4426_-2-4383del
ENST00000467482.5:c.250+316_250+359del	ENSP00000417161.1:n.250+316_250+359del
NM_000273.2:c.250+316_250+359del	NP_000264.2:n.250+316_250+359del
XM_005274541.2:c.250+316_250+359del	XP_005274598.1:n.250+316_250+359del
XM_005274541.3:c.250+316_250+359del	XP_005274598.1:n.250+316_250+359del
XM_024452387.1:c.-2-4426_-2-4383del	XP_024308155.1:n.-2-4426_-2-4383del
XM_024452388.1:c.-2-4426_-2-4383del	XP_024308156.1:n.-2-4426_-2-4383del
NM_000273.3:c.250+316_250+359del MANE Select	NP_000264.2:n.250+316_250+359del