Canonical Allele Identifier: CA329462970

Gene: MAOA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43688062A>G , CM000685.2:g.43688062A>G	GRCh38
NC_000023.10:g.43547310A>G , CM000685.1:g.43547310A>G	GRCh37
NC_000023.9:g.43432254A>G	NCBI36
NG_008957.2:g.36902A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497485.2:n.300+4455A>G
ENST00000542639.6:c.-232+4455A>G	ENSP00000440846.1:n.-232+4455A>G
ENST00000686683.1:c.-443+4455A>G	ENSP00000509063.1:n.-443+4455A>G
ENST00000686980.1:n.300+4455A>G
ENST00000688006.1:c.-232+4455A>G	ENSP00000510311.1:n.-232+4455A>G
ENST00000689087.1:c.-232+4455A>G	ENSP00000508997.1:n.-232+4455A>G
ENST00000693128.1:c.168+4455A>G	ENSP00000508493.1:n.168+4455A>G
ENST00000338702.4:c.168+4455A>G MANE Select	ENSP00000340684.3:n.168+4455A>G
ENST00000338702.3:c.168+4455A>G	ENSP00000340684.3:n.168+4455A>G
ENST00000497485.1:n.316+4455A>G
ENST00000542639.5:c.-232+4455A>G	ENSP00000440846.1:n.-232+4455A>G
NM_000240.3:c.168+4455A>G	NP_000231.1:n.168+4455A>G
NM_001270458.1:c.-232+4455A>G	NP_001257387.1:n.-232+4455A>G
NM_000240.4:c.168+4455A>G MANE Select	NP_000231.1:n.168+4455A>G
NM_001270458.2:c.-232+4455A>G	NP_001257387.1:n.-232+4455A>G