Canonical Allele Identifier: CA2819650393
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765623_9765624insA , CM000685.2:g.9765623_9765624insA GRCh38
NC_000023.10:g.9733663_9733664insA , CM000685.1:g.9733663_9733664insA GRCh37
NC_000023.9:g.9693663_9693664insA NCBI36
NG_009074.1:g.5254_5255insT

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.194_195insT MANE Select ENSP00000417161.1:p.Ala66GlyfsTer?
ENST00000431126.1:c.-3+496_-3+497insT ENSP00000406138.1:n.-3+496_-3+497insT
ENST00000447366.5:c.-2-4798_-2-4797insT ENSP00000390546.2:n.-2-4798_-2-4797insT
ENST00000467482.5:c.194_195insT ENSP00000417161.1:p.Ala66GlyfsTer?
NM_000273.2:c.194_195insT NP_000264.2:p.Ala66GlyfsTer?
XM_005274541.2:c.194_195insT XP_005274598.1:p.Ala66GlyfsTer?
XM_005274541.3:c.194_195insT XP_005274598.1:p.Ala66GlyfsTer?
XM_024452387.1:c.-2-4798_-2-4797insT XP_024308155.1:n.-2-4798_-2-4797insT
XM_024452388.1:c.-2-4798_-2-4797insT XP_024308156.1:n.-2-4798_-2-4797insT
NM_000273.3:c.194_195insT MANE Select NP_000264.2:p.Ala66GlyfsTer?