Canonical Allele Identifier: CA880029600

Gene: GPR143

Linked Data

• dbSNP Id: rs1273037223
• gnomAD v3: X-9741075-T-G
• gnomAD v4: X-9741075-T-G
• MyVariant Identifiers: chrX:g.9709115T>G (hg19) ; chrX:g.9741075T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741075T>G , CM000685.2:g.9741075T>G	GRCh38
NC_000023.10:g.9709115T>G , CM000685.1:g.9709115T>G	GRCh37
NC_000023.9:g.9669115T>G	NCBI36
NG_009074.1:g.29803A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+263A>C MANE Select	ENSP00000417161.1:n.885+263A>C
ENST00000447366.5:c.633+263A>C	ENSP00000390546.2:n.633+263A>C
ENST00000467482.5:c.885+263A>C	ENSP00000417161.1:n.885+263A>C
NM_000273.2:c.885+263A>C	NP_000264.2:n.885+263A>C
XM_005274541.2:c.885+263A>C	XP_005274598.1:n.885+263A>C
XM_005274541.3:c.885+263A>C	XP_005274598.1:n.885+263A>C
XM_024452387.1:c.633+263A>C	XP_024308155.1:n.633+263A>C
XM_024452388.1:c.633+263A>C	XP_024308156.1:n.633+263A>C
NM_000273.3:c.885+263A>C MANE Select	NP_000264.2:n.885+263A>C