Canonical Allele Identifier: CA2693068835

Gene: GPR143

Linked Data

• gnomAD v4: X-9741089-A-AGACGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741089_9741090insGACGGC , CM000685.2:g.9741089_9741090insGACGGC	GRCh38
NC_000023.10:g.9709129_9709130insGACGGC , CM000685.1:g.9709129_9709130insGACGGC	GRCh37
NC_000023.9:g.9669129_9669130insGACGGC	NCBI36
NG_009074.1:g.29788_29789insGCCGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+248_885+249insGCCGTC MANE Select	ENSP00000417161.1:n.885+248_885+249insGCCGTC
ENST00000447366.5:c.633+248_633+249insGCCGTC	ENSP00000390546.2:n.633+248_633+249insGCCGTC
ENST00000467482.5:c.885+248_885+249insGCCGTC	ENSP00000417161.1:n.885+248_885+249insGCCGTC
NM_000273.2:c.885+248_885+249insGCCGTC	NP_000264.2:n.885+248_885+249insGCCGTC
XM_005274541.2:c.885+248_885+249insGCCGTC	XP_005274598.1:n.885+248_885+249insGCCGTC
XM_005274541.3:c.885+248_885+249insGCCGTC	XP_005274598.1:n.885+248_885+249insGCCGTC
XM_024452387.1:c.633+248_633+249insGCCGTC	XP_024308155.1:n.633+248_633+249insGCCGTC
XM_024452388.1:c.633+248_633+249insGCCGTC	XP_024308156.1:n.633+248_633+249insGCCGTC
NM_000273.3:c.885+248_885+249insGCCGTC MANE Select	NP_000264.2:n.885+248_885+249insGCCGTC