Canonical Allele Identifier: CA880114443

Gene: GPR143

Linked Data

• dbSNP Id: rs1253996179
• gnomAD v3: X-9765549-G-A
• gnomAD v4: X-9765549-G-A
• MyVariant Identifiers: chrX:g.9733589G>A (hg19) ; chrX:g.9765549G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765549G>A , CM000685.2:g.9765549G>A	GRCh38
NC_000023.10:g.9733589G>A , CM000685.1:g.9733589G>A	GRCh37
NC_000023.9:g.9693589G>A	NCBI36
NG_009074.1:g.5329C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+19C>T MANE Select	ENSP00000417161.1:n.250+19C>T
ENST00000431126.1:c.-3+571C>T	ENSP00000406138.1:n.-3+571C>T
ENST00000447366.5:c.-2-4723C>T	ENSP00000390546.2:n.-2-4723C>T
ENST00000467482.5:c.250+19C>T	ENSP00000417161.1:n.250+19C>T
NM_000273.2:c.250+19C>T	NP_000264.2:n.250+19C>T
XM_005274541.2:c.250+19C>T	XP_005274598.1:n.250+19C>T
XM_005274541.3:c.250+19C>T	XP_005274598.1:n.250+19C>T
XM_024452387.1:c.-2-4723C>T	XP_024308155.1:n.-2-4723C>T
XM_024452388.1:c.-2-4723C>T	XP_024308156.1:n.-2-4723C>T
NM_000273.3:c.250+19C>T MANE Select	NP_000264.2:n.250+19C>T