Canonical Allele Identifier: CA1130984065

Gene: GPR143

Linked Data

• gnomAD v3: X-9765244-C-CCG
• gnomAD v4: X-9765244-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765245_9765246insGC , CM000685.2:g.9765245_9765246insGC	GRCh38
NC_000023.10:g.9733285_9733286insGC , CM000685.1:g.9733285_9733286insGC	GRCh37
NC_000023.9:g.9693285_9693286insGC	NCBI36
NG_009074.1:g.5633_5634insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+323_250+324insCG MANE Select	ENSP00000417161.1:n.250+323_250+324insCG
ENST00000431126.1:c.-3+875_-3+876insCG	ENSP00000406138.1:n.-3+875_-3+876insCG
ENST00000447366.5:c.-2-4419_-2-4418insCG	ENSP00000390546.2:n.-2-4419_-2-4418insCG
ENST00000467482.5:c.250+323_250+324insCG	ENSP00000417161.1:n.250+323_250+324insCG
NM_000273.2:c.250+323_250+324insCG	NP_000264.2:n.250+323_250+324insCG
XM_005274541.2:c.250+323_250+324insCG	XP_005274598.1:n.250+323_250+324insCG
XM_005274541.3:c.250+323_250+324insCG	XP_005274598.1:n.250+323_250+324insCG
XM_024452387.1:c.-2-4419_-2-4418insCG	XP_024308155.1:n.-2-4419_-2-4418insCG
XM_024452388.1:c.-2-4419_-2-4418insCG	XP_024308156.1:n.-2-4419_-2-4418insCG
NM_000273.3:c.250+323_250+324insCG MANE Select	NP_000264.2:n.250+323_250+324insCG