Canonical Allele Identifier: CA2693068909

Gene: GPR143

Linked Data

• gnomAD v4: X-9741216-A-AATCG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741217_9741218insTCGA , CM000685.2:g.9741217_9741218insTCGA	GRCh38
NC_000023.10:g.9709257_9709258insTCGA , CM000685.1:g.9709257_9709258insTCGA	GRCh37
NC_000023.9:g.9669257_9669258insTCGA	NCBI36
NG_009074.1:g.29661_29662insCGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+121_885+122insCGAT MANE Select	ENSP00000417161.1:n.885+121_885+122insCGAT
ENST00000447366.5:c.633+121_633+122insCGAT	ENSP00000390546.2:n.633+121_633+122insCGAT
ENST00000467482.5:c.885+121_885+122insCGAT	ENSP00000417161.1:n.885+121_885+122insCGAT
NM_000273.2:c.885+121_885+122insCGAT	NP_000264.2:n.885+121_885+122insCGAT
XM_005274541.2:c.885+121_885+122insCGAT	XP_005274598.1:n.885+121_885+122insCGAT
XM_005274541.3:c.885+121_885+122insCGAT	XP_005274598.1:n.885+121_885+122insCGAT
XM_024452387.1:c.633+121_633+122insCGAT	XP_024308155.1:n.633+121_633+122insCGAT
XM_024452388.1:c.633+121_633+122insCGAT	XP_024308156.1:n.633+121_633+122insCGAT
NM_000273.3:c.885+121_885+122insCGAT MANE Select	NP_000264.2:n.885+121_885+122insCGAT