Canonical Allele Identifier: CA411995893
Gene: GPR143 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741380C>A , CM000685.2:g.9741380C>A GRCh38
NC_000023.10:g.9709420C>A , CM000685.1:g.9709420C>A GRCh37
NC_000023.9:g.9669420C>A NCBI36
NG_009074.1:g.29498G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.843G>T MANE Select ENSP00000417161.1:p.Leu281Phe
ENST00000447366.5:c.591G>T ENSP00000390546.2:p.Leu197Phe
ENST00000467482.5:c.843G>T ENSP00000417161.1:p.Leu281Phe
NM_000273.2:c.843G>T NP_000264.2:p.Leu281Phe
XM_005274541.2:c.843G>T XP_005274598.1:p.Leu281Phe
XM_005274541.3:c.843G>T XP_005274598.1:p.Leu281Phe
XM_024452387.1:c.591G>T XP_024308155.1:p.Leu197Phe
XM_024452388.1:c.591G>T XP_024308156.1:p.Leu197Phe
NM_000273.3:c.843G>T MANE Select NP_000264.2:p.Leu281Phe