Canonical Allele Identifier: CA2476076591
Gene: DDAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.85433825A= , CM000663.2:g.85433825A= GRCh38
NC_000001.10:g.85899508A= , CM000663.1:g.85899508A= GRCh37
NC_000001.9:g.85672096A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000284031.13:c.303+30918T= MANE Select ENSP00000284031.8:n.303+30918T=
ENST00000426972.8:c.-7+62341T= ENSP00000411189.4:n.-7+62341T=
ENST00000284031.12:c.303+30918T= ENSP00000284031.8:n.303+30918T=
ENST00000426972.7:c.-7+62341T= ENSP00000411189.4:n.-7+62341T=
ENST00000483110.5:n.383+62341T=
ENST00000535924.6:c.-7+62341T= ENSP00000439045.1:n.-7+62341T=
ENST00000539042.3:c.303+30918T= ENSP00000438604.1:n.303+30918T=
NM_001134445.1:c.-7+62341T= NP_001127917.1:n.-7+62341T=
NM_012137.3:c.303+30918T= NP_036269.1:n.303+30918T=
XM_005270707.2:c.19-74978T= XP_005270764.1:n.19-74978T=
XM_005270709.2:c.-7+62341T= XP_005270766.1:n.-7+62341T=
XM_011541158.1:c.-87+62341T= XP_011539460.1:n.-87+62341T=
XM_017000889.1:c.24+30671T= XP_016856378.1:n.24+30671T=
XM_024446130.1:c.-7+62341T= XP_024301898.1:n.-7+62341T=
NM_012137.4:c.303+30918T= MANE Select NP_036269.1:n.303+30918T=
NM_001134445.2:c.-7+62341T= NP_001127917.1:n.-7+62341T=