Canonical Allele Identifier: CA10390779

Gene: MAOA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43712692C>T , CM000685.2:g.43712692C>T	GRCh38
NC_000023.10:g.43571939C>T , CM000685.1:g.43571939C>T	GRCh37
NC_000023.9:g.43456883C>T	NCBI36
NG_008957.2:g.61532C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000240.4:c.412-13C>T MANE Select	NP_000231.1:n.412-13C>T
ENST00000338702.4:c.412-13C>T MANE Select	ENSP00000340684.3:n.412-13C>T
NM_000240.3:c.412-13C>T	NP_000231.1:n.412-13C>T
NM_001270458.1:c.13-13C>T	NP_001257387.1:n.13-13C>T
NM_001270458.2:c.13-13C>T	NP_001257387.1:n.13-13C>T
ENST00000338702.3:c.412-13C>T	ENSP00000340684.3:n.412-13C>T
ENST00000497485.1:n.560-13C>T
ENST00000542639.5:c.13-13C>T	ENSP00000440846.1:n.13-13C>T
ENST00000542639.6:c.13-13C>T	ENSP00000440846.1:n.13-13C>T
ENST00000686683.1:c.-199-13C>T	ENSP00000509063.1:n.-199-13C>T
ENST00000686980.1:n.544-13C>T
ENST00000688006.1:c.13-13C>T	ENSP00000510311.1:n.13-13C>T
ENST00000689087.1:c.13-13C>T	ENSP00000508997.1:n.13-13C>T
ENST00000693128.1:c.307-13C>T	ENSP00000508493.1:n.307-13C>T