Canonical Allele Identifier: CA326092547
Gene: GPR143 HGNC NCBI

Linked Data

dbSNP Id: rs767590684
MyVariant Identifiers: chrX:g.9709082del (hg19) chrX:g.9741042del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741043del , CM000685.2:g.9741043del GRCh38
NC_000023.10:g.9709083del , CM000685.1:g.9709083del GRCh37
NC_000023.9:g.9669083del NCBI36
NG_009074.1:g.29836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+296del MANE Select ENSP00000417161.1:n.885+296del
ENST00000447366.5:c.633+296del ENSP00000390546.2:n.633+296del
ENST00000467482.5:c.885+296del ENSP00000417161.1:n.885+296del
NM_000273.2:c.885+296del NP_000264.2:n.885+296del
XM_005274541.2:c.885+296del XP_005274598.1:n.885+296del
XR_950507.1:n.297del
XM_005274541.3:c.885+296del XP_005274598.1:n.885+296del
XM_024452387.1:c.633+296del XP_024308155.1:n.633+296del
XM_024452388.1:c.633+296del XP_024308156.1:n.633+296del
NM_000273.3:c.885+296del MANE Select NP_000264.2:n.885+296del
Search 100 bp 5'
Search 100 bp 3'