Canonical Allele Identifier: CA412000499

Gene: GPR143

Linked Data

• MyVariant Identifiers: chrX:g.9733661G>C (hg19) ; chrX:g.9765621G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765621G>C , CM000685.2:g.9765621G>C	GRCh38
NC_000023.10:g.9733661G>C , CM000685.1:g.9733661G>C	GRCh37
NC_000023.9:g.9693661G>C	NCBI36
NG_009074.1:g.5257C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.197C>G MANE Select	ENSP00000417161.1:p.Ala66Gly
ENST00000431126.1:c.-3+499C>G	ENSP00000406138.1:n.-3+499C>G
ENST00000447366.5:c.-2-4795C>G	ENSP00000390546.2:n.-2-4795C>G
ENST00000467482.5:c.197C>G	ENSP00000417161.1:p.Ala66Gly
NM_000273.2:c.197C>G	NP_000264.2:p.Ala66Gly
XM_005274541.2:c.197C>G	XP_005274598.1:p.Ala66Gly
XM_005274541.3:c.197C>G	XP_005274598.1:p.Ala66Gly
XM_024452387.1:c.-2-4795C>G	XP_024308155.1:n.-2-4795C>G
XM_024452388.1:c.-2-4795C>G	XP_024308156.1:n.-2-4795C>G
NM_000273.3:c.197C>G MANE Select	NP_000264.2:p.Ala66Gly