Canonical Allele Identifier: CA880029594

Gene: GPR143 TBL1X

Linked Data

• dbSNP Id: rs1186445188
• gnomAD v3: X-9741035-T-A
• gnomAD v4: X-9741035-T-A
• MyVariant Identifiers: chrX:g.9709075T>A (hg19) ; chrX:g.9741035T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741035T>A , CM000685.2:g.9741035T>A	GRCh38
NC_000023.10:g.9709075T>A , CM000685.1:g.9709075T>A	GRCh37
NC_000023.9:g.9669075T>A	NCBI36
NG_009074.1:g.29843A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+303A>T (GPR143) MANE Select	ENSP00000417161.1:n.885+303A>T
ENST00000647060.1:c.*227T>A (TBL1X)	ENSP00000495467.1:n.*227T>A
ENST00000447366.5:c.633+303A>T (GPR143)	ENSP00000390546.2:n.633+303A>T
ENST00000467482.5:c.885+303A>T (GPR143)	ENSP00000417161.1:n.885+303A>T
NM_000273.2:c.885+303A>T (GPR143)	NP_000264.2:n.885+303A>T
XM_005274541.2:c.885+303A>T (GPR143)	XP_005274598.1:n.885+303A>T
XR_950507.1:n.289T>A
XM_005274541.3:c.885+303A>T (GPR143)	XP_005274598.1:n.885+303A>T
XM_024452387.1:c.633+303A>T (GPR143)	XP_024308155.1:n.633+303A>T
XM_024452388.1:c.633+303A>T (GPR143)	XP_024308156.1:n.633+303A>T
NM_000273.3:c.885+303A>T (GPR143) MANE Select	NP_000264.2:n.885+303A>T