Canonical Allele Identifier: CA1320725796

Gene: AOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200661607A= , CM000664.2:g.200661607A=	GRCh38
NC_000002.11:g.201526330A= , CM000664.1:g.201526330A=	GRCh37
NC_000002.10:g.201234575A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001159.4:c.3404A= MANE Select	NP_001150.3:p.Asn1135=
ENST00000374700.7:c.3404A= MANE Select	ENSP00000363832.2:p.Asn1135=
NM_001159.3:c.3404A=	NP_001150.3:p.Asn1135=
ENST00000260930.10:c.62A=	ENSP00000260930.6:p.Asn21=
ENST00000374700.6:c.3404A=	ENSP00000363832.2:p.Asn1135=
ENST00000465297.5:n.2336A=
ENST00000485106.5:n.2143A=
XM_011511062.1:c.3404A=	XP_011509364.1:p.Asn1135=
XM_017003946.1:c.3404A=	XP_016859435.1:p.Asn1135=
XM_017003947.2:c.3404A=	XP_016859436.1:p.Asn1135=
XR_922913.1:n.3561A=