Canonical Allele Identifier: CA2693068816
Gene: GPR143 HGNC NCBI

Linked Data

gnomAD v4: X-9741053-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741053A>G , CM000685.2:g.9741053A>G GRCh38
NC_000023.10:g.9709093A>G , CM000685.1:g.9709093A>G GRCh37
NC_000023.9:g.9669093A>G NCBI36
NG_009074.1:g.29825T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+285T>C MANE Select ENSP00000417161.1:n.885+285T>C
ENST00000447366.5:c.633+285T>C ENSP00000390546.2:n.633+285T>C
ENST00000467482.5:c.885+285T>C ENSP00000417161.1:n.885+285T>C
NM_000273.2:c.885+285T>C NP_000264.2:n.885+285T>C
XM_005274541.2:c.885+285T>C XP_005274598.1:n.885+285T>C
XR_950507.1:n.307A>G
XM_005274541.3:c.885+285T>C XP_005274598.1:n.885+285T>C
XM_024452387.1:c.633+285T>C XP_024308155.1:n.633+285T>C
XM_024452388.1:c.633+285T>C XP_024308156.1:n.633+285T>C
NM_000273.3:c.885+285T>C MANE Select NP_000264.2:n.885+285T>C
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