Canonical Allele Identifier: CA2693068908

Gene: GPR143

Linked Data

• gnomAD v4: X-9741215-T-TGAGACCAGCCTGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741215_9741216insGAGACCAGCCTGGGC , CM000685.2:g.9741215_9741216insGAGACCAGCCTGGGC	GRCh38
NC_000023.10:g.9709255_9709256insGAGACCAGCCTGGGC , CM000685.1:g.9709255_9709256insGAGACCAGCCTGGGC	GRCh37
NC_000023.9:g.9669255_9669256insGAGACCAGCCTGGGC	NCBI36
NG_009074.1:g.29662_29663insGCCCAGGCTGGTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+122_885+123insGCCCAGGCTGGTCTC MANE Select	ENSP00000417161.1:n.885+122_885+123insGCCCAGGCTGGTCTC
ENST00000447366.5:c.633+122_633+123insGCCCAGGCTGGTCTC	ENSP00000390546.2:n.633+122_633+123insGCCCAGGCTGGTCTC
ENST00000467482.5:c.885+122_885+123insGCCCAGGCTGGTCTC	ENSP00000417161.1:n.885+122_885+123insGCCCAGGCTGGTCTC
NM_000273.2:c.885+122_885+123insGCCCAGGCTGGTCTC	NP_000264.2:n.885+122_885+123insGCCCAGGCTGGTCTC
XM_005274541.2:c.885+122_885+123insGCCCAGGCTGGTCTC	XP_005274598.1:n.885+122_885+123insGCCCAGGCTGGTCTC
XM_005274541.3:c.885+122_885+123insGCCCAGGCTGGTCTC	XP_005274598.1:n.885+122_885+123insGCCCAGGCTGGTCTC
XM_024452387.1:c.633+122_633+123insGCCCAGGCTGGTCTC	XP_024308155.1:n.633+122_633+123insGCCCAGGCTGGTCTC
XM_024452388.1:c.633+122_633+123insGCCCAGGCTGGTCTC	XP_024308156.1:n.633+122_633+123insGCCCAGGCTGGTCTC
NM_000273.3:c.885+122_885+123insGCCCAGGCTGGTCTC MANE Select	NP_000264.2:n.885+122_885+123insGCCCAGGCTGGTCTC