Canonical Allele Identifier: CA880029614
Gene: GPR143 HGNC NCBI

Linked Data

dbSNP Id: rs1259097611
MyVariant Identifiers: chrX:g.9709209A>C (hg19) chrX:g.9741169A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741169A>C , CM000685.2:g.9741169A>C GRCh38
NC_000023.10:g.9709209A>C , CM000685.1:g.9709209A>C GRCh37
NC_000023.9:g.9669209A>C NCBI36
NG_009074.1:g.29709T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+169T>G MANE Select ENSP00000417161.1:n.885+169T>G
ENST00000447366.5:c.633+169T>G ENSP00000390546.2:n.633+169T>G
ENST00000467482.5:c.885+169T>G ENSP00000417161.1:n.885+169T>G
NM_000273.2:c.885+169T>G NP_000264.2:n.885+169T>G
XM_005274541.2:c.885+169T>G XP_005274598.1:n.885+169T>G
XM_005274541.3:c.885+169T>G XP_005274598.1:n.885+169T>G
XM_024452387.1:c.633+169T>G XP_024308155.1:n.633+169T>G
XM_024452388.1:c.633+169T>G XP_024308156.1:n.633+169T>G
NM_000273.3:c.885+169T>G MANE Select NP_000264.2:n.885+169T>G
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