Canonical Allele Identifier: CA2819650346

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765116_9765123del , CM000685.2:g.9765116_9765123del	GRCh38
NC_000023.10:g.9733156_9733163del , CM000685.1:g.9733156_9733163del	GRCh37
NC_000023.9:g.9693156_9693163del	NCBI36
NG_009074.1:g.5756_5763del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+446_250+453del MANE Select	ENSP00000417161.1:n.250+446_250+453del
ENST00000431126.1:c.-3+998_-3+1005del	ENSP00000406138.1:n.-3+998_-3+1005del
ENST00000447366.5:c.-2-4296_-2-4289del	ENSP00000390546.2:n.-2-4296_-2-4289del
ENST00000467482.5:c.250+446_250+453del	ENSP00000417161.1:n.250+446_250+453del
NM_000273.2:c.250+446_250+453del	NP_000264.2:n.250+446_250+453del
XM_005274541.2:c.250+446_250+453del	XP_005274598.1:n.250+446_250+453del
XM_005274541.3:c.250+446_250+453del	XP_005274598.1:n.250+446_250+453del
XM_024452387.1:c.-2-4296_-2-4289del	XP_024308155.1:n.-2-4296_-2-4289del
XM_024452388.1:c.-2-4296_-2-4289del	XP_024308156.1:n.-2-4296_-2-4289del
NM_000273.3:c.250+446_250+453del MANE Select	NP_000264.2:n.250+446_250+453del