Canonical Allele Identifier: CA2415024325
Gene: GPR143 HGNC NCBI

Linked Data

dbSNP Id: rs1362703730
gnomAD v4: X-9741091-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741091G>A , CM000685.2:g.9741091G>A GRCh38
NC_000023.10:g.9709131G>A , CM000685.1:g.9709131G>A GRCh37
NC_000023.9:g.9669131G>A NCBI36
NG_009074.1:g.29787C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+247C>T MANE Select ENSP00000417161.1:n.885+247C>T
ENST00000447366.5:c.633+247C>T ENSP00000390546.2:n.633+247C>T
ENST00000467482.5:c.885+247C>T ENSP00000417161.1:n.885+247C>T
NM_000273.2:c.885+247C>T NP_000264.2:n.885+247C>T
XM_005274541.2:c.885+247C>T XP_005274598.1:n.885+247C>T
XM_005274541.3:c.885+247C>T XP_005274598.1:n.885+247C>T
XM_024452387.1:c.633+247C>T XP_024308155.1:n.633+247C>T
XM_024452388.1:c.633+247C>T XP_024308156.1:n.633+247C>T
NM_000273.3:c.885+247C>T MANE Select NP_000264.2:n.885+247C>T