Canonical Allele Identifier: CA2693068901
Gene: GPR143 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741212_9741215del , CM000685.2:g.9741212_9741215del GRCh38
NC_000023.10:g.9709252_9709255del , CM000685.1:g.9709252_9709255del GRCh37
NC_000023.9:g.9669252_9669255del NCBI36
NG_009074.1:g.29663_29666del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+123_885+126del MANE Select ENSP00000417161.1:n.885+123_885+126del
ENST00000447366.5:c.633+123_633+126del ENSP00000390546.2:n.633+123_633+126del
ENST00000467482.5:c.885+123_885+126del ENSP00000417161.1:n.885+123_885+126del
NM_000273.2:c.885+123_885+126del NP_000264.2:n.885+123_885+126del
XM_005274541.2:c.885+123_885+126del XP_005274598.1:n.885+123_885+126del
XM_005274541.3:c.885+123_885+126del XP_005274598.1:n.885+123_885+126del
XM_024452387.1:c.633+123_633+126del XP_024308155.1:n.633+123_633+126del
XM_024452388.1:c.633+123_633+126del XP_024308156.1:n.633+123_633+126del
NM_000273.3:c.885+123_885+126del MANE Select NP_000264.2:n.885+123_885+126del