Canonical Allele Identifier: CA1130984023
Gene: GPR143 HGNC NCBI

Linked Data

dbSNP Id: rs2083523325
gnomAD v3: X-9765069-G-A
gnomAD v4: X-9765069-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765069G>A , CM000685.2:g.9765069G>A GRCh38
NC_000023.10:g.9733109G>A , CM000685.1:g.9733109G>A GRCh37
NC_000023.9:g.9693109G>A NCBI36
NG_009074.1:g.5809C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.250+499C>T MANE Select ENSP00000417161.1:n.250+499C>T
ENST00000431126.1:c.-3+1051C>T ENSP00000406138.1:n.-3+1051C>T
ENST00000447366.5:c.-2-4243C>T ENSP00000390546.2:n.-2-4243C>T
ENST00000467482.5:c.250+499C>T ENSP00000417161.1:n.250+499C>T
NM_000273.2:c.250+499C>T NP_000264.2:n.250+499C>T
XM_005274541.2:c.250+499C>T XP_005274598.1:n.250+499C>T
XM_005274541.3:c.250+499C>T XP_005274598.1:n.250+499C>T
XM_024452387.1:c.-2-4243C>T XP_024308155.1:n.-2-4243C>T
XM_024452388.1:c.-2-4243C>T XP_024308156.1:n.-2-4243C>T
NM_000273.3:c.250+499C>T MANE Select NP_000264.2:n.250+499C>T