Canonical Allele Identifier: CA1130974806
Gene: GPR143 HGNC NCBI

Linked Data

dbSNP Id: rs2083402223
gnomAD v3: X-9741174-C-G
gnomAD v4: X-9741174-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741174C>G , CM000685.2:g.9741174C>G GRCh38
NC_000023.10:g.9709214C>G , CM000685.1:g.9709214C>G GRCh37
NC_000023.9:g.9669214C>G NCBI36
NG_009074.1:g.29704G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+164G>C MANE Select ENSP00000417161.1:n.885+164G>C
ENST00000447366.5:c.633+164G>C ENSP00000390546.2:n.633+164G>C
ENST00000467482.5:c.885+164G>C ENSP00000417161.1:n.885+164G>C
NM_000273.2:c.885+164G>C NP_000264.2:n.885+164G>C
XM_005274541.2:c.885+164G>C XP_005274598.1:n.885+164G>C
XM_005274541.3:c.885+164G>C XP_005274598.1:n.885+164G>C
XM_024452387.1:c.633+164G>C XP_024308155.1:n.633+164G>C
XM_024452388.1:c.633+164G>C XP_024308156.1:n.633+164G>C
NM_000273.3:c.885+164G>C MANE Select NP_000264.2:n.885+164G>C
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