Canonical Allele Identifier: CA2693067406

Gene: GPR143

Linked Data

• gnomAD v4: X-9765420-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765424_9765425del , CM000685.2:g.9765424_9765425del	GRCh38
NC_000023.10:g.9733464_9733465del , CM000685.1:g.9733464_9733465del	GRCh37
NC_000023.9:g.9693464_9693465del	NCBI36
NG_009074.1:g.5456_5457del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+146_250+147del MANE Select	ENSP00000417161.1:n.250+146_250+147del
ENST00000431126.1:c.-3+698_-3+699del	ENSP00000406138.1:n.-3+698_-3+699del
ENST00000447366.5:c.-2-4596_-2-4595del	ENSP00000390546.2:n.-2-4596_-2-4595del
ENST00000467482.5:c.250+146_250+147del	ENSP00000417161.1:n.250+146_250+147del
NM_000273.2:c.250+146_250+147del	NP_000264.2:n.250+146_250+147del
XM_005274541.2:c.250+146_250+147del	XP_005274598.1:n.250+146_250+147del
XM_005274541.3:c.250+146_250+147del	XP_005274598.1:n.250+146_250+147del
XM_024452387.1:c.-2-4596_-2-4595del	XP_024308155.1:n.-2-4596_-2-4595del
XM_024452388.1:c.-2-4596_-2-4595del	XP_024308156.1:n.-2-4596_-2-4595del
NM_000273.3:c.250+146_250+147del MANE Select	NP_000264.2:n.250+146_250+147del