Canonical Allele Identifier: CA2693067561

Gene: GPR143

Linked Data

• gnomAD v4: X-9765517-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765518del , CM000685.2:g.9765518del	GRCh38
NC_000023.10:g.9733558del , CM000685.1:g.9733558del	GRCh37
NC_000023.9:g.9693558del	NCBI36
NG_009074.1:g.5360del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+50del MANE Select	ENSP00000417161.1:n.250+50del
ENST00000431126.1:c.-3+602del	ENSP00000406138.1:n.-3+602del
ENST00000447366.5:c.-2-4692del	ENSP00000390546.2:n.-2-4692del
ENST00000467482.5:c.250+50del	ENSP00000417161.1:n.250+50del
NM_000273.2:c.250+50del	NP_000264.2:n.250+50del
XM_005274541.2:c.250+50del	XP_005274598.1:n.250+50del
XM_005274541.3:c.250+50del	XP_005274598.1:n.250+50del
XM_024452387.1:c.-2-4692del	XP_024308155.1:n.-2-4692del
XM_024452388.1:c.-2-4692del	XP_024308156.1:n.-2-4692del
NM_000273.3:c.250+50del MANE Select	NP_000264.2:n.250+50del