Canonical Allele Identifier: CA2693509045

Gene: MAOA

Linked Data

• gnomAD v4: X-43731888-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731888T>C , CM000685.2:g.43731888T>C	GRCh38
NC_000023.10:g.43591135T>C , CM000685.1:g.43591135T>C	GRCh37
NC_000023.9:g.43476079T>C	NCBI36
NG_008957.2:g.80728T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.556+35T>C	ENSP00000440846.1:n.556+35T>C
ENST00000686683.1:c.265+35T>C	ENSP00000509063.1:n.265+35T>C
ENST00000686980.1:n.1087+35T>C
ENST00000688006.1:c.556+35T>C	ENSP00000510311.1:n.556+35T>C
ENST00000688859.1:n.511+35T>C
ENST00000689087.1:c.556+35T>C	ENSP00000508997.1:n.556+35T>C
ENST00000693128.1:c.850+35T>C	ENSP00000508493.1:n.850+35T>C
ENST00000338702.4:c.955+35T>C MANE Select	ENSP00000340684.3:n.955+35T>C
ENST00000338702.3:c.955+35T>C	ENSP00000340684.3:n.955+35T>C
ENST00000542639.5:c.556+35T>C	ENSP00000440846.1:n.556+35T>C
NM_000240.3:c.955+35T>C	NP_000231.1:n.955+35T>C
NM_001270458.1:c.556+35T>C	NP_001257387.1:n.556+35T>C
NM_000240.4:c.955+35T>C MANE Select	NP_000231.1:n.955+35T>C
NM_001270458.2:c.556+35T>C	NP_001257387.1:n.556+35T>C