Canonical Allele Identifier: CA10390847

Gene: MAOA

Linked Data

• dbSNP Id: rs780527254
• ExAC: X:43590975 T / C
• gnomAD v2: X-43590975-T-C
• MyVariant Identifiers: chrX:g.43590975T>C (hg19) ; chrX:g.43731728T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731728T>C , CM000685.2:g.43731728T>C	GRCh38
NC_000023.10:g.43590975T>C , CM000685.1:g.43590975T>C	GRCh37
NC_000023.9:g.43475919T>C	NCBI36
NG_008957.2:g.80568T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.431T>C	ENSP00000440846.1:p.Leu144Ser
ENST00000686683.1:c.140T>C	ENSP00000509063.1:p.Leu47Ser
ENST00000686980.1:n.962T>C
ENST00000688006.1:c.431T>C	ENSP00000510311.1:p.Leu144Ser
ENST00000688859.1:n.386T>C
ENST00000689087.1:c.431T>C	ENSP00000508997.1:p.Leu144Ser
ENST00000693128.1:c.725T>C	ENSP00000508493.1:p.Leu242Ser
ENST00000338702.4:c.830T>C MANE Select	ENSP00000340684.3:p.Leu277Ser
ENST00000338702.3:c.830T>C	ENSP00000340684.3:p.Leu277Ser
ENST00000542639.5:c.431T>C	ENSP00000440846.1:p.Leu144Ser
NM_000240.3:c.830T>C	NP_000231.1:p.Leu277Ser
NM_001270458.1:c.431T>C	NP_001257387.1:p.Leu144Ser
NM_000240.4:c.830T>C MANE Select	NP_000231.1:p.Leu277Ser
NM_001270458.2:c.431T>C	NP_001257387.1:p.Leu144Ser