Canonical Allele Identifier: CA2476032488

Gene: DDAH1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85321306A= , CM000663.2:g.85321306A=	GRCh38
NC_000001.10:g.85786989A= , CM000663.1:g.85786989A=	GRCh37
NC_000001.9:g.85559577A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284031.13:c.*146T= MANE Select	ENSP00000284031.8:n.*146T=
ENST00000426972.8:c.*146T=	ENSP00000411189.4:n.*146T=
ENST00000284031.12:c.*146T=	ENSP00000284031.8:n.*146T=
ENST00000426972.7:c.*146T=	ENSP00000411189.4:n.*146T=
ENST00000483110.5:n.1084T=
ENST00000535924.6:c.*146T=	ENSP00000439045.1:n.*146T=
ENST00000539042.3:c.*146T=	ENSP00000438604.1:n.*146T=
NM_001134445.1:c.*146T=	NP_001127917.1:n.*146T=
NM_012137.3:c.*146T=	NP_036269.1:n.*146T=
XM_005270707.2:c.*146T=	XP_005270764.1:n.*146T=
XM_005270709.2:c.*146T=	XP_005270766.1:n.*146T=
XM_005270710.2:c.*146T=	XP_005270767.1:n.*146T=
XM_006710544.1:c.*146T=	XP_006710607.1:n.*146T=
XM_011541158.1:c.*146T=	XP_011539460.1:n.*146T=
NM_001330655.1:c.*146T=	NP_001317584.1:n.*146T=
XM_017000889.1:c.*146T=	XP_016856378.1:n.*146T=
XM_024446130.1:c.*146T=	XP_024301898.1:n.*146T=
NM_012137.4:c.*146T= MANE Select	NP_036269.1:n.*146T=
NM_001134445.2:c.*146T=	NP_001127917.1:n.*146T=
NM_001330655.2:c.*146T=	NP_001317584.1:n.*146T=