Canonical Allele Identifier: CA640485001

Gene: GPR143

Linked Data

• dbSNP Id: rs1321717158
• gnomAD v2: X-9709080-T-C
• gnomAD v3: X-9741040-T-C
• gnomAD v4: X-9741040-T-C
• MyVariant Identifiers: chrX:g.9709080T>C (hg19) ; chrX:g.9741040T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741040T>C , CM000685.2:g.9741040T>C	GRCh38
NC_000023.10:g.9709080T>C , CM000685.1:g.9709080T>C	GRCh37
NC_000023.9:g.9669080T>C	NCBI36
NG_009074.1:g.29838A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+298A>G MANE Select	ENSP00000417161.1:n.885+298A>G
ENST00000447366.5:c.633+298A>G	ENSP00000390546.2:n.633+298A>G
ENST00000467482.5:c.885+298A>G	ENSP00000417161.1:n.885+298A>G
NM_000273.2:c.885+298A>G	NP_000264.2:n.885+298A>G
XM_005274541.2:c.885+298A>G	XP_005274598.1:n.885+298A>G
XR_950507.1:n.294T>C
XM_005274541.3:c.885+298A>G	XP_005274598.1:n.885+298A>G
XM_024452387.1:c.633+298A>G	XP_024308155.1:n.633+298A>G
XM_024452388.1:c.633+298A>G	XP_024308156.1:n.633+298A>G
NM_000273.3:c.885+298A>G MANE Select	NP_000264.2:n.885+298A>G