Canonical Allele Identifier: CA2693068840
Gene: GPR143 HGNC NCBI

Linked Data

gnomAD v4: X-9741093-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741093G>T , CM000685.2:g.9741093G>T GRCh38
NC_000023.10:g.9709133G>T , CM000685.1:g.9709133G>T GRCh37
NC_000023.9:g.9669133G>T NCBI36
NG_009074.1:g.29785C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+245C>A MANE Select ENSP00000417161.1:n.885+245C>A
ENST00000447366.5:c.633+245C>A ENSP00000390546.2:n.633+245C>A
ENST00000467482.5:c.885+245C>A ENSP00000417161.1:n.885+245C>A
NM_000273.2:c.885+245C>A NP_000264.2:n.885+245C>A
XM_005274541.2:c.885+245C>A XP_005274598.1:n.885+245C>A
XM_005274541.3:c.885+245C>A XP_005274598.1:n.885+245C>A
XM_024452387.1:c.633+245C>A XP_024308155.1:n.633+245C>A
XM_024452388.1:c.633+245C>A XP_024308156.1:n.633+245C>A
NM_000273.3:c.885+245C>A MANE Select NP_000264.2:n.885+245C>A
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