Canonical Allele Identifier: CA880029609

Gene: GPR143

Linked Data

• dbSNP Id: rs1411559707
• gnomAD v3: X-9741127-C-G
• gnomAD v4: X-9741127-C-G
• MyVariant Identifiers: chrX:g.9709167C>G (hg19) ; chrX:g.9741127C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741127C>G , CM000685.2:g.9741127C>G	GRCh38
NC_000023.10:g.9709167C>G , CM000685.1:g.9709167C>G	GRCh37
NC_000023.9:g.9669167C>G	NCBI36
NG_009074.1:g.29751G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+211G>C MANE Select	ENSP00000417161.1:n.885+211G>C
ENST00000447366.5:c.633+211G>C	ENSP00000390546.2:n.633+211G>C
ENST00000467482.5:c.885+211G>C	ENSP00000417161.1:n.885+211G>C
NM_000273.2:c.885+211G>C	NP_000264.2:n.885+211G>C
XM_005274541.2:c.885+211G>C	XP_005274598.1:n.885+211G>C
XM_005274541.3:c.885+211G>C	XP_005274598.1:n.885+211G>C
XM_024452387.1:c.633+211G>C	XP_024308155.1:n.633+211G>C
XM_024452388.1:c.633+211G>C	XP_024308156.1:n.633+211G>C
NM_000273.3:c.885+211G>C MANE Select	NP_000264.2:n.885+211G>C