Canonical Allele Identifier: CA880114390

Gene: GPR143

Linked Data

• dbSNP Id: rs1200045151
• MyVariant Identifiers: chrX:g.9733583_9733600del (hg19) ; chrX:g.9765543_9765560del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765543_9765560del , CM000685.2:g.9765543_9765560del	GRCh38
NC_000023.10:g.9733583_9733600del , CM000685.1:g.9733583_9733600del	GRCh37
NC_000023.9:g.9693583_9693600del	NCBI36
NG_009074.1:g.5318_5335del

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+8_250+25del MANE Select	ENSP00000417161.1:n.250+8_250+25del
ENST00000431126.1:c.-3+560_-3+577del	ENSP00000406138.1:n.-3+560_-3+577del
ENST00000447366.5:c.-2-4734_-2-4717del	ENSP00000390546.2:n.-2-4734_-2-4717del
ENST00000467482.5:c.250+8_250+25del	ENSP00000417161.1:n.250+8_250+25del
NM_000273.2:c.250+8_250+25del	NP_000264.2:n.250+8_250+25del
XM_005274541.2:c.250+8_250+25del	XP_005274598.1:n.250+8_250+25del
XM_005274541.3:c.250+8_250+25del	XP_005274598.1:n.250+8_250+25del
XM_024452387.1:c.-2-4734_-2-4717del	XP_024308155.1:n.-2-4734_-2-4717del
XM_024452388.1:c.-2-4734_-2-4717del	XP_024308156.1:n.-2-4734_-2-4717del
NM_000273.3:c.250+8_250+25del MANE Select	NP_000264.2:n.250+8_250+25del