Canonical Allele Identifier: CA326107062

Gene: GPR143

Linked Data

• dbSNP Id: rs35358584
• MyVariant Identifiers: chrX:g.9733299_9733300insG (hg19) ; chrX:g.9765259_9765260insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765263dup , CM000685.2:g.9765263dup	GRCh38
NC_000023.10:g.9733303dup , CM000685.1:g.9733303dup	GRCh37
NC_000023.9:g.9693303dup	NCBI36
NG_009074.1:g.5618dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+308dup MANE Select	ENSP00000417161.1:n.250+308dup
ENST00000431126.1:c.-3+860dup	ENSP00000406138.1:n.-3+860dup
ENST00000447366.5:c.-2-4434dup	ENSP00000390546.2:n.-2-4434dup
ENST00000467482.5:c.250+308dup	ENSP00000417161.1:n.250+308dup
NM_000273.2:c.250+308dup	NP_000264.2:n.250+308dup
XM_005274541.2:c.250+308dup	XP_005274598.1:n.250+308dup
XM_005274541.3:c.250+308dup	XP_005274598.1:n.250+308dup
XM_024452387.1:c.-2-4434dup	XP_024308155.1:n.-2-4434dup
XM_024452388.1:c.-2-4434dup	XP_024308156.1:n.-2-4434dup
NM_000273.3:c.250+308dup MANE Select	NP_000264.2:n.250+308dup