Canonical Allele Identifier: CA500228828

Gene: AOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42852621T>G , CM000679.2:g.42852621T>G	GRCh38
NC_000017.10:g.41004638T>G , CM000679.1:g.41004638T>G	GRCh37
NC_000017.9:g.38258164T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003734.4:c.1278T>G MANE Select	NP_003725.1:p.Arg426=
ENST00000308423.7:c.1278T>G MANE Select	ENSP00000312326.1:p.Arg426=
NM_001277731.1:c.1278T>G	NP_001264660.1:p.Arg426=
NM_001277731.2:c.1278T>G	NP_001264660.1:p.Arg426=
NM_003734.3:c.1278T>G	NP_003725.1:p.Arg426=
NR_102422.1:n.1438T>G
NR_102422.2:n.1423T>G
ENST00000308423.6:c.1278T>G	ENSP00000312326.1:p.Arg426=
ENST00000613571.1:c.1278T>G	ENSP00000484312.1:p.Arg426=
XM_011525419.1:c.1278T>G	XP_011523721.1:p.Arg426=
XM_011525419.2:c.1278T>G	XP_011523721.1:p.Arg426=
XM_011525420.1:c.1278T>G	XP_011523722.1:p.Arg426=
XM_011525420.3:c.1278T>G	XP_011523722.1:p.Arg426=
XR_001752673.2:n.1440T>G
XR_934584.1:n.1499T>G
XR_934584.2:n.1440T>G