Canonical Allele Identifier: CA880029615

Gene: GPR143

Linked Data

• dbSNP Id: rs1189110044
• MyVariant Identifiers: chrX:g.9709213_9709216del (hg19) ; chrX:g.9741173_9741176del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741174_9741177del , CM000685.2:g.9741174_9741177del	GRCh38
NC_000023.10:g.9709214_9709217del , CM000685.1:g.9709214_9709217del	GRCh37
NC_000023.9:g.9669214_9669217del	NCBI36
NG_009074.1:g.29702_29705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+162_885+165del MANE Select	ENSP00000417161.1:n.885+162_885+165del
ENST00000447366.5:c.633+162_633+165del	ENSP00000390546.2:n.633+162_633+165del
ENST00000467482.5:c.885+162_885+165del	ENSP00000417161.1:n.885+162_885+165del
NM_000273.2:c.885+162_885+165del	NP_000264.2:n.885+162_885+165del
XM_005274541.2:c.885+162_885+165del	XP_005274598.1:n.885+162_885+165del
XM_005274541.3:c.885+162_885+165del	XP_005274598.1:n.885+162_885+165del
XM_024452387.1:c.633+162_633+165del	XP_024308155.1:n.633+162_633+165del
XM_024452388.1:c.633+162_633+165del	XP_024308156.1:n.633+162_633+165del
NM_000273.3:c.885+162_885+165del MANE Select	NP_000264.2:n.885+162_885+165del