Canonical Allele Identifier: CA640485000

Gene: GPR143 TBL1X

Linked Data

• dbSNP Id: rs1262857813
• gnomAD v2: X-9709070-A-G
• gnomAD v3: X-9741030-A-G
• gnomAD v4: X-9741030-A-G
• MyVariant Identifiers: chrX:g.9709070A>G (hg19) ; chrX:g.9741030A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741030A>G , CM000685.2:g.9741030A>G	GRCh38
NC_000023.10:g.9709070A>G , CM000685.1:g.9709070A>G	GRCh37
NC_000023.9:g.9669070A>G	NCBI36
NG_009074.1:g.29848T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+308T>C (GPR143) MANE Select	ENSP00000417161.1:n.885+308T>C
ENST00000647060.1:c.*222A>G (TBL1X)	ENSP00000495467.1:n.*222A>G
ENST00000447366.5:c.633+308T>C (GPR143)	ENSP00000390546.2:n.633+308T>C
ENST00000467482.5:c.885+308T>C (GPR143)	ENSP00000417161.1:n.885+308T>C
NM_000273.2:c.885+308T>C (GPR143)	NP_000264.2:n.885+308T>C
XM_005274541.2:c.885+308T>C (GPR143)	XP_005274598.1:n.885+308T>C
XR_950507.1:n.284A>G
XM_005274541.3:c.885+308T>C (GPR143)	XP_005274598.1:n.885+308T>C
XM_024452387.1:c.633+308T>C (GPR143)	XP_024308155.1:n.633+308T>C
XM_024452388.1:c.633+308T>C (GPR143)	XP_024308156.1:n.633+308T>C
NM_000273.3:c.885+308T>C (GPR143) MANE Select	NP_000264.2:n.885+308T>C