Canonical Allele Identifier: CA2819654739

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9741225_9741226insCC , CM000685.2:g.9741225_9741226insCC	GRCh38
NC_000023.10:g.9709265_9709266insCC , CM000685.1:g.9709265_9709266insCC	GRCh37
NC_000023.9:g.9669265_9669266insCC	NCBI36
NG_009074.1:g.29652_29653insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.885+112_885+113insGG MANE Select	ENSP00000417161.1:n.885+112_885+113insGG
ENST00000447366.5:c.633+112_633+113insGG	ENSP00000390546.2:n.633+112_633+113insGG
ENST00000467482.5:c.885+112_885+113insGG	ENSP00000417161.1:n.885+112_885+113insGG
NM_000273.2:c.885+112_885+113insGG	NP_000264.2:n.885+112_885+113insGG
XM_005274541.2:c.885+112_885+113insGG	XP_005274598.1:n.885+112_885+113insGG
XM_005274541.3:c.885+112_885+113insGG	XP_005274598.1:n.885+112_885+113insGG
XM_024452387.1:c.633+112_633+113insGG	XP_024308155.1:n.633+112_633+113insGG
XM_024452388.1:c.633+112_633+113insGG	XP_024308156.1:n.633+112_633+113insGG
NM_000273.3:c.885+112_885+113insGG MANE Select	NP_000264.2:n.885+112_885+113insGG