Canonical Allele Identifier: CA2415024312
Gene: GPR143 HGNC NCBI

Linked Data

dbSNP Id: rs2083401445

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741044G>C , CM000685.2:g.9741044G>C GRCh38
NC_000023.10:g.9709084G>C , CM000685.1:g.9709084G>C GRCh37
NC_000023.9:g.9669084G>C NCBI36
NG_009074.1:g.29834C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+294C>G MANE Select ENSP00000417161.1:n.885+294C>G
ENST00000447366.5:c.633+294C>G ENSP00000390546.2:n.633+294C>G
ENST00000467482.5:c.885+294C>G ENSP00000417161.1:n.885+294C>G
NM_000273.2:c.885+294C>G NP_000264.2:n.885+294C>G
XM_005274541.2:c.885+294C>G XP_005274598.1:n.885+294C>G
XR_950507.1:n.298G>C
XM_005274541.3:c.885+294C>G XP_005274598.1:n.885+294C>G
XM_024452387.1:c.633+294C>G XP_024308155.1:n.633+294C>G
XM_024452388.1:c.633+294C>G XP_024308156.1:n.633+294C>G
NM_000273.3:c.885+294C>G MANE Select NP_000264.2:n.885+294C>G