Canonical Allele Identifier: CA10391035

Gene: MAOB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43767586A>G , CM000685.2:g.43767586A>G	GRCh38
NC_000023.10:g.43626833A>G , CM000685.1:g.43626833A>G	GRCh37
NC_000023.9:g.43511777A>G	NCBI36
NG_008723.1:g.119889T>C
NG_008723.2:g.119890T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378069.5:c.1443T>C MANE Select	ENSP00000367309.4:p.Phe481=
ENST00000378069.4:c.1443T>C	ENSP00000367309.4:p.Phe481=
NM_000898.4:c.1443T>C	NP_000889.3:p.Phe481=
XM_005272607.3:c.1395T>C	XP_005272664.1:p.Phe465=
XM_005272608.2:c.1395T>C	XP_005272665.1:p.Phe465=
XM_011543914.1:c.1305T>C	XP_011542216.1:p.Phe435=
XM_005272608.3:c.1395T>C	XP_005272665.1:p.Phe465=
XM_017029523.1:c.1395T>C	XP_016885012.1:p.Phe465=
XM_017029524.2:c.1395T>C	XP_016885013.1:p.Phe465=
NM_000898.5:c.1443T>C MANE Select	NP_000889.3:p.Phe481=