Canonical Allele Identifier: CA1139921648

Gene: DDAH1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85350451T= , CM000663.2:g.85350451T=	GRCh38
NC_000001.10:g.85816134T= , CM000663.1:g.85816134T=	GRCh37
NC_000001.9:g.85588722T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284031.13:c.561A= MANE Select	ENSP00000284031.8:p.Ala187=
ENST00000426972.8:c.252A=	ENSP00000411189.4:p.Ala84=
ENST00000284031.12:c.561A=	ENSP00000284031.8:p.Ala187=
ENST00000426972.7:c.252A=	ENSP00000411189.4:p.Ala84=
ENST00000483110.5:n.641A=
ENST00000535924.6:c.252A=	ENSP00000439045.1:p.Ala84=
ENST00000539042.3:c.561A=	ENSP00000438604.1:p.Ala187=
ENST00000633113.1:c.261A=	ENSP00000488725.1:p.Ala87=
NM_001134445.1:c.252A=	NP_001127917.1:p.Ala84=
NM_012137.3:c.561A=	NP_036269.1:p.Ala187=
XM_005270707.2:c.276A=	XP_005270764.1:p.Ala92=
XM_005270709.2:c.252A=	XP_005270766.1:p.Ala84=
XM_005270710.2:c.252A=	XP_005270767.1:p.Ala84=
XM_006710544.1:c.252A=	XP_006710607.1:p.Ala84=
XM_011541158.1:c.261A=	XP_011539460.1:p.Ala87=
NM_001330655.1:c.261A=	NP_001317584.1:p.Ala87=
XM_017000889.1:c.282A=	XP_016856378.1:p.Ala94=
XM_024446130.1:c.252A=	XP_024301898.1:p.Ala84=
NM_012137.4:c.561A= MANE Select	NP_036269.1:p.Ala187=
NM_001134445.2:c.252A=	NP_001127917.1:p.Ala84=
NM_001330655.2:c.261A=	NP_001317584.1:p.Ala87=