Canonical Allele Identifier: CA2693068810

Gene: GPR143

Linked Data

• gnomAD v4: X-9741027-TTTAAATATAATATATTGTACTTCTGACTGCTTCTTTTTCTTCTGATTTTTTTTCAAGCAGAAAGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741037_9741102del , CM000685.2:g.9741037_9741102del	GRCh38
NC_000023.10:g.9709077_9709142del , CM000685.1:g.9709077_9709142del	GRCh37
NC_000023.9:g.9669077_9669142del	NCBI36
NG_009074.1:g.29785_29850del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+245_885+310del MANE Select	ENSP00000417161.1:n.885+245_885+310del
ENST00000447366.5:c.633+245_633+310del	ENSP00000390546.2:n.633+245_633+310del
ENST00000467482.5:c.885+245_885+310del	ENSP00000417161.1:n.885+245_885+310del
NM_000273.2:c.885+245_885+310del	NP_000264.2:n.885+245_885+310del
XM_005274541.2:c.885+245_885+310del	XP_005274598.1:n.885+245_885+310del
XM_005274541.3:c.885+245_885+310del	XP_005274598.1:n.885+245_885+310del
XM_024452387.1:c.633+245_633+310del	XP_024308155.1:n.633+245_633+310del
XM_024452388.1:c.633+245_633+310del	XP_024308156.1:n.633+245_633+310del
NM_000273.3:c.885+245_885+310del MANE Select	NP_000264.2:n.885+245_885+310del