Canonical Allele Identifier: CA273042

Gene: GPR143

Linked Data

• ClinVar Variation Id: 162039
• ClinVar RCV Id: RCV000149456
• dbSNP Id: rs672601353
• MyVariant Identifiers: chrX:g.9733635dupC (hg19) ; chrX:g.9733634_9733635insC (hg19) ; chrX:g.9765595dupC (hg38) ; chrX:g.9765594_9765595insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765595dup , CM000685.2:g.9765595dup	GRCh38
NC_000023.10:g.9733635dup , CM000685.1:g.9733635dup	GRCh37
NC_000023.9:g.9693635dup	NCBI36
NG_009074.1:g.5283dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.223dup MANE Select	ENSP00000417161.1:p.Ala75GlyfsTer26
ENST00000431126.1:c.-3+525dup	ENSP00000406138.1:n.-3+525dup
ENST00000447366.5:c.-2-4769dup	ENSP00000390546.2:n.-2-4769dup
ENST00000467482.5:c.223dup	ENSP00000417161.1:p.Ala75GlyfsTer26
NM_000273.2:c.223dup	NP_000264.2:p.Ala75GlyfsTer26
XM_005274541.2:c.223dup	XP_005274598.1:p.Ala75GlyfsTer26
XM_005274541.3:c.223dup	XP_005274598.1:p.Ala75GlyfsTer26
XM_024452387.1:c.-2-4769dup	XP_024308155.1:n.-2-4769dup
XM_024452388.1:c.-2-4769dup	XP_024308156.1:n.-2-4769dup
NM_000273.3:c.223dup MANE Select	NP_000264.2:p.Ala75GlyfsTer26