Canonical Allele Identifier: CA2415024329
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741109_9741110delinsTA , CM000685.2:g.9741109_9741110delinsTA GRCh38
NC_000023.10:g.9709149_9709150delinsTA , CM000685.1:g.9709149_9709150delinsTA GRCh37
NC_000023.9:g.9669149_9669150delinsTA NCBI36
NG_009074.1:g.29768_29769delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+228_885+229delinsTA MANE Select ENSP00000417161.1:n.885+228_885+229delinsTA
ENST00000447366.5:c.633+228_633+229delinsTA ENSP00000390546.2:n.633+228_633+229delinsTA
ENST00000467482.5:c.885+228_885+229delinsTA ENSP00000417161.1:n.885+228_885+229delinsTA
NM_000273.2:c.885+228_885+229delinsTA NP_000264.2:n.885+228_885+229delinsTA
XM_005274541.2:c.885+228_885+229delinsTA XP_005274598.1:n.885+228_885+229delinsTA
XM_005274541.3:c.885+228_885+229delinsTA XP_005274598.1:n.885+228_885+229delinsTA
XM_024452387.1:c.633+228_633+229delinsTA XP_024308155.1:n.633+228_633+229delinsTA
XM_024452388.1:c.633+228_633+229delinsTA XP_024308156.1:n.633+228_633+229delinsTA
NM_000273.3:c.885+228_885+229delinsTA MANE Select NP_000264.2:n.885+228_885+229delinsTA