Canonical Allele Identifier: CA2693068912

Gene: GPR143

Linked Data

• gnomAD v4: X-9741217-A-AGACCAGCCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741218_9741219insACCAGCCTGG , CM000685.2:g.9741218_9741219insACCAGCCTGG	GRCh38
NC_000023.10:g.9709258_9709259insACCAGCCTGG , CM000685.1:g.9709258_9709259insACCAGCCTGG	GRCh37
NC_000023.9:g.9669258_9669259insACCAGCCTGG	NCBI36
NG_009074.1:g.29660_29661insCAGGCTGGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+120_885+121insCAGGCTGGTC MANE Select	ENSP00000417161.1:n.885+120_885+121insCAGGCTGGTC
ENST00000447366.5:c.633+120_633+121insCAGGCTGGTC	ENSP00000390546.2:n.633+120_633+121insCAGGCTGGTC
ENST00000467482.5:c.885+120_885+121insCAGGCTGGTC	ENSP00000417161.1:n.885+120_885+121insCAGGCTGGTC
NM_000273.2:c.885+120_885+121insCAGGCTGGTC	NP_000264.2:n.885+120_885+121insCAGGCTGGTC
XM_005274541.2:c.885+120_885+121insCAGGCTGGTC	XP_005274598.1:n.885+120_885+121insCAGGCTGGTC
XM_005274541.3:c.885+120_885+121insCAGGCTGGTC	XP_005274598.1:n.885+120_885+121insCAGGCTGGTC
XM_024452387.1:c.633+120_633+121insCAGGCTGGTC	XP_024308155.1:n.633+120_633+121insCAGGCTGGTC
XM_024452388.1:c.633+120_633+121insCAGGCTGGTC	XP_024308156.1:n.633+120_633+121insCAGGCTGGTC
NM_000273.3:c.885+120_885+121insCAGGCTGGTC MANE Select	NP_000264.2:n.885+120_885+121insCAGGCTGGTC