Canonical Allele Identifier: CA412000503

Gene: GPR143

Linked Data

• MyVariant Identifiers: chrX:g.9733662C>G (hg19) ; chrX:g.9765622C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765622C>G , CM000685.2:g.9765622C>G	GRCh38
NC_000023.10:g.9733662C>G , CM000685.1:g.9733662C>G	GRCh37
NC_000023.9:g.9693662C>G	NCBI36
NG_009074.1:g.5256G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.196G>C MANE Select	ENSP00000417161.1:p.Ala66Pro
ENST00000431126.1:c.-3+498G>C	ENSP00000406138.1:n.-3+498G>C
ENST00000447366.5:c.-2-4796G>C	ENSP00000390546.2:n.-2-4796G>C
ENST00000467482.5:c.196G>C	ENSP00000417161.1:p.Ala66Pro
NM_000273.2:c.196G>C	NP_000264.2:p.Ala66Pro
XM_005274541.2:c.196G>C	XP_005274598.1:p.Ala66Pro
XM_005274541.3:c.196G>C	XP_005274598.1:p.Ala66Pro
XM_024452387.1:c.-2-4796G>C	XP_024308155.1:n.-2-4796G>C
XM_024452388.1:c.-2-4796G>C	XP_024308156.1:n.-2-4796G>C
NM_000273.3:c.196G>C MANE Select	NP_000264.2:p.Ala66Pro