Canonical Allele Identifier: CA2693068917

Gene: GPR143

Linked Data

• gnomAD v4: X-9741220-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741221_9741222del , CM000685.2:g.9741221_9741222del	GRCh38
NC_000023.10:g.9709261_9709262del , CM000685.1:g.9709261_9709262del	GRCh37
NC_000023.9:g.9669261_9669262del	NCBI36
NG_009074.1:g.29656_29657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+116_885+117del MANE Select	ENSP00000417161.1:n.885+116_885+117del
ENST00000447366.5:c.633+116_633+117del	ENSP00000390546.2:n.633+116_633+117del
ENST00000467482.5:c.885+116_885+117del	ENSP00000417161.1:n.885+116_885+117del
NM_000273.2:c.885+116_885+117del	NP_000264.2:n.885+116_885+117del
XM_005274541.2:c.885+116_885+117del	XP_005274598.1:n.885+116_885+117del
XM_005274541.3:c.885+116_885+117del	XP_005274598.1:n.885+116_885+117del
XM_024452387.1:c.633+116_633+117del	XP_024308155.1:n.633+116_633+117del
XM_024452388.1:c.633+116_633+117del	XP_024308156.1:n.633+116_633+117del
NM_000273.3:c.885+116_885+117del MANE Select	NP_000264.2:n.885+116_885+117del