Canonical Allele Identifier: CA350269807

Gene: AOX1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_001159.4:c.3404A>C MANE Select	NP_001150.3:p.Asn1135Thr
ENST00000374700.7:c.3404A>C MANE Select	ENSP00000363832.2:p.Asn1135Thr
NM_001159.3:c.3404A>C	NP_001150.3:p.Asn1135Thr
ENST00000260930.10:c.62A>C	ENSP00000260930.6:p.Asn21Thr
ENST00000374700.6:c.3404A>C	ENSP00000363832.2:p.Asn1135Thr
ENST00000465297.5:n.2336A>C
ENST00000485106.5:n.2143A>C
XM_011511062.1:c.3404A>C	XP_011509364.1:p.Asn1135Thr
XM_017003946.1:c.3404A>C	XP_016859435.1:p.Asn1135Thr
XM_017003947.2:c.3404A>C	XP_016859436.1:p.Asn1135Thr
XR_922913.1:n.3561A>C