Canonical Allele Identifier: CA326092549

Gene: GPR143

Linked Data

• dbSNP Id: rs756204978
• gnomAD v2: X-9709092-G-A
• gnomAD v3: X-9741052-G-A
• gnomAD v4: X-9741052-G-A
• MyVariant Identifiers: chrX:g.9709092G>A (hg19) ; chrX:g.9741052G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741052G>A , CM000685.2:g.9741052G>A	GRCh38
NC_000023.10:g.9709092G>A , CM000685.1:g.9709092G>A	GRCh37
NC_000023.9:g.9669092G>A	NCBI36
NG_009074.1:g.29826C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+286C>T MANE Select	ENSP00000417161.1:n.885+286C>T
ENST00000447366.5:c.633+286C>T	ENSP00000390546.2:n.633+286C>T
ENST00000467482.5:c.885+286C>T	ENSP00000417161.1:n.885+286C>T
NM_000273.2:c.885+286C>T	NP_000264.2:n.885+286C>T
XM_005274541.2:c.885+286C>T	XP_005274598.1:n.885+286C>T
XR_950507.1:n.306G>A
XM_005274541.3:c.885+286C>T	XP_005274598.1:n.885+286C>T
XM_024452387.1:c.633+286C>T	XP_024308155.1:n.633+286C>T
XM_024452388.1:c.633+286C>T	XP_024308156.1:n.633+286C>T
NM_000273.3:c.885+286C>T MANE Select	NP_000264.2:n.885+286C>T