Canonical Allele Identifier: CA2819650380
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765499A>C , CM000685.2:g.9765499A>C GRCh38
NC_000023.10:g.9733539A>C , CM000685.1:g.9733539A>C GRCh37
NC_000023.9:g.9693539A>C NCBI36
NG_009074.1:g.5379T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.250+69T>G MANE Select ENSP00000417161.1:n.250+69T>G
ENST00000431126.1:c.-3+621T>G ENSP00000406138.1:n.-3+621T>G
ENST00000447366.5:c.-2-4673T>G ENSP00000390546.2:n.-2-4673T>G
ENST00000467482.5:c.250+69T>G ENSP00000417161.1:n.250+69T>G
NM_000273.2:c.250+69T>G NP_000264.2:n.250+69T>G
XM_005274541.2:c.250+69T>G XP_005274598.1:n.250+69T>G
XM_005274541.3:c.250+69T>G XP_005274598.1:n.250+69T>G
XM_024452387.1:c.-2-4673T>G XP_024308155.1:n.-2-4673T>G
XM_024452388.1:c.-2-4673T>G XP_024308156.1:n.-2-4673T>G
NM_000273.3:c.250+69T>G MANE Select NP_000264.2:n.250+69T>G