Canonical Allele Identifier: CA2415032467
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765554G= , CM000685.2:g.9765554G= GRCh38
NC_000023.10:g.9733594G= , CM000685.1:g.9733594G= GRCh37
NC_000023.9:g.9693594G= NCBI36
NG_009074.1:g.5324C=

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.250+14C= MANE Select ENSP00000417161.1:n.250+14C=
ENST00000431126.1:c.-3+566C= ENSP00000406138.1:n.-3+566C=
ENST00000447366.5:c.-2-4728C= ENSP00000390546.2:n.-2-4728C=
ENST00000467482.5:c.250+14C= ENSP00000417161.1:n.250+14C=
NM_000273.2:c.250+14C= NP_000264.2:n.250+14C=
XM_005274541.2:c.250+14C= XP_005274598.1:n.250+14C=
XM_005274541.3:c.250+14C= XP_005274598.1:n.250+14C=
XM_024452387.1:c.-2-4728C= XP_024308155.1:n.-2-4728C=
XM_024452388.1:c.-2-4728C= XP_024308156.1:n.-2-4728C=
NM_000273.3:c.250+14C= MANE Select NP_000264.2:n.250+14C=