Canonical Allele Identifier: CA412000791

Gene: GPR143

Linked Data

• gnomAD v4: X-9765729-T-C
• MyVariant Identifiers: chrX:g.9733769T>C (hg19) ; chrX:g.9765729T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765729T>C , CM000685.2:g.9765729T>C	GRCh38
NC_000023.10:g.9733769T>C , CM000685.1:g.9733769T>C	GRCh37
NC_000023.9:g.9693769T>C	NCBI36
NG_009074.1:g.5149A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.89A>G MANE Select	ENSP00000417161.1:p.His30Arg
ENST00000431126.1:c.-3+391A>G	ENSP00000406138.1:n.-3+391A>G
ENST00000447366.5:c.-2-4903A>G	ENSP00000390546.2:n.-2-4903A>G
ENST00000467482.5:c.89A>G	ENSP00000417161.1:p.His30Arg
NM_000273.2:c.89A>G	NP_000264.2:p.His30Arg
XM_005274541.2:c.89A>G	XP_005274598.1:p.His30Arg
XM_005274541.3:c.89A>G	XP_005274598.1:p.His30Arg
XM_024452387.1:c.-2-4903A>G	XP_024308155.1:n.-2-4903A>G
XM_024452388.1:c.-2-4903A>G	XP_024308156.1:n.-2-4903A>G
NM_000273.3:c.89A>G MANE Select	NP_000264.2:p.His30Arg