Canonical Allele Identifier: CA412000481

Gene: GPR143

Linked Data

• MyVariant Identifiers: chrX:g.9733655A>T (hg19) ; chrX:g.9765615A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765615A>T , CM000685.2:g.9765615A>T	GRCh38
NC_000023.10:g.9733655A>T , CM000685.1:g.9733655A>T	GRCh37
NC_000023.9:g.9693655A>T	NCBI36
NG_009074.1:g.5263T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.203T>A MANE Select	ENSP00000417161.1:p.Val68Asp
ENST00000431126.1:c.-3+505T>A	ENSP00000406138.1:n.-3+505T>A
ENST00000447366.5:c.-2-4789T>A	ENSP00000390546.2:n.-2-4789T>A
ENST00000467482.5:c.203T>A	ENSP00000417161.1:p.Val68Asp
NM_000273.2:c.203T>A	NP_000264.2:p.Val68Asp
XM_005274541.2:c.203T>A	XP_005274598.1:p.Val68Asp
XM_005274541.3:c.203T>A	XP_005274598.1:p.Val68Asp
XM_024452387.1:c.-2-4789T>A	XP_024308155.1:n.-2-4789T>A
XM_024452388.1:c.-2-4789T>A	XP_024308156.1:n.-2-4789T>A
NM_000273.3:c.203T>A MANE Select	NP_000264.2:p.Val68Asp