Canonical Allele Identifier: CA329461595

Gene: MAOA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43667695A>C , CM000685.2:g.43667695A>C	GRCh38
NC_000023.10:g.43526943A>C , CM000685.1:g.43526943A>C	GRCh37
NC_000023.9:g.43411887A>C	NCBI36
NG_008957.2:g.16535A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497485.2:n.205+11281A>C
ENST00000542639.6:c.-327+9726A>C	ENSP00000440846.1:n.-327+9726A>C
ENST00000686683.1:c.-538+9726A>C	ENSP00000509063.1:n.-538+9726A>C
ENST00000686980.1:n.205+11281A>C
ENST00000688006.1:c.-327+11233A>C	ENSP00000510311.1:n.-327+11233A>C
ENST00000689087.1:c.-327+11336A>C	ENSP00000508997.1:n.-327+11336A>C
ENST00000693128.1:c.73+11281A>C	ENSP00000508493.1:n.73+11281A>C
ENST00000338702.4:c.73+11281A>C MANE Select	ENSP00000340684.3:n.73+11281A>C
ENST00000338702.3:c.73+11281A>C	ENSP00000340684.3:n.73+11281A>C
ENST00000497485.1:n.221+9726A>C
ENST00000542639.5:c.-327+9726A>C	ENSP00000440846.1:n.-327+9726A>C
NM_000240.3:c.73+11281A>C	NP_000231.1:n.73+11281A>C
NM_001270458.1:c.-327+9726A>C	NP_001257387.1:n.-327+9726A>C
NM_000240.4:c.73+11281A>C MANE Select	NP_000231.1:n.73+11281A>C
NM_001270458.2:c.-327+9726A>C	NP_001257387.1:n.-327+9726A>C