Canonical Allele Identifier: CA2819654691

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741081_9741089del , CM000685.2:g.9741081_9741089del	GRCh38
NC_000023.10:g.9709121_9709129del , CM000685.1:g.9709121_9709129del	GRCh37
NC_000023.9:g.9669121_9669129del	NCBI36
NG_009074.1:g.29789_29797del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+249_885+257del MANE Select	ENSP00000417161.1:n.885+249_885+257del
ENST00000447366.5:c.633+249_633+257del	ENSP00000390546.2:n.633+249_633+257del
ENST00000467482.5:c.885+249_885+257del	ENSP00000417161.1:n.885+249_885+257del
NM_000273.2:c.885+249_885+257del	NP_000264.2:n.885+249_885+257del
XM_005274541.2:c.885+249_885+257del	XP_005274598.1:n.885+249_885+257del
XM_005274541.3:c.885+249_885+257del	XP_005274598.1:n.885+249_885+257del
XM_024452387.1:c.633+249_633+257del	XP_024308155.1:n.633+249_633+257del
XM_024452388.1:c.633+249_633+257del	XP_024308156.1:n.633+249_633+257del
NM_000273.3:c.885+249_885+257del MANE Select	NP_000264.2:n.885+249_885+257del