Canonical Allele Identifier: CA2693068907

Gene: GPR143

Linked Data

• gnomAD v4: X-9741213-T-TCTGAGACCAGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741213_9741214insCTGAGACCAGCC , CM000685.2:g.9741213_9741214insCTGAGACCAGCC	GRCh38
NC_000023.10:g.9709253_9709254insCTGAGACCAGCC , CM000685.1:g.9709253_9709254insCTGAGACCAGCC	GRCh37
NC_000023.9:g.9669253_9669254insCTGAGACCAGCC	NCBI36
NG_009074.1:g.29664_29665insGGCTGGTCTCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+124_885+125insGGCTGGTCTCAG MANE Select	ENSP00000417161.1:n.885+124_885+125insGGCTGGTCTCAG
ENST00000447366.5:c.633+124_633+125insGGCTGGTCTCAG	ENSP00000390546.2:n.633+124_633+125insGGCTGGTCTCAG
ENST00000467482.5:c.885+124_885+125insGGCTGGTCTCAG	ENSP00000417161.1:n.885+124_885+125insGGCTGGTCTCAG
NM_000273.2:c.885+124_885+125insGGCTGGTCTCAG	NP_000264.2:n.885+124_885+125insGGCTGGTCTCAG
XM_005274541.2:c.885+124_885+125insGGCTGGTCTCAG	XP_005274598.1:n.885+124_885+125insGGCTGGTCTCAG
XM_005274541.3:c.885+124_885+125insGGCTGGTCTCAG	XP_005274598.1:n.885+124_885+125insGGCTGGTCTCAG
XM_024452387.1:c.633+124_633+125insGGCTGGTCTCAG	XP_024308155.1:n.633+124_633+125insGGCTGGTCTCAG
XM_024452388.1:c.633+124_633+125insGGCTGGTCTCAG	XP_024308156.1:n.633+124_633+125insGGCTGGTCTCAG
NM_000273.3:c.885+124_885+125insGGCTGGTCTCAG MANE Select	NP_000264.2:n.885+124_885+125insGGCTGGTCTCAG