Canonical Allele Identifier: CA2476076563
Gene: DDAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.85433743C= , CM000663.2:g.85433743C= GRCh38
NC_000001.10:g.85899426C= , CM000663.1:g.85899426C= GRCh37
NC_000001.9:g.85672014C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000284031.13:c.303+31000G= MANE Select ENSP00000284031.8:n.303+31000G=
ENST00000426972.8:c.-7+62423G= ENSP00000411189.4:n.-7+62423G=
ENST00000284031.12:c.303+31000G= ENSP00000284031.8:n.303+31000G=
ENST00000426972.7:c.-7+62423G= ENSP00000411189.4:n.-7+62423G=
ENST00000483110.5:n.383+62423G=
ENST00000535924.6:c.-7+62423G= ENSP00000439045.1:n.-7+62423G=
ENST00000539042.3:c.303+31000G= ENSP00000438604.1:n.303+31000G=
NM_001134445.1:c.-7+62423G= NP_001127917.1:n.-7+62423G=
NM_012137.3:c.303+31000G= NP_036269.1:n.303+31000G=
XM_005270707.2:c.19-74896G= XP_005270764.1:n.19-74896G=
XM_005270709.2:c.-7+62423G= XP_005270766.1:n.-7+62423G=
XM_011541158.1:c.-87+62423G= XP_011539460.1:n.-87+62423G=
XM_017000889.1:c.24+30753G= XP_016856378.1:n.24+30753G=
XM_024446130.1:c.-7+62423G= XP_024301898.1:n.-7+62423G=
NM_012137.4:c.303+31000G= MANE Select NP_036269.1:n.303+31000G=
NM_001134445.2:c.-7+62423G= NP_001127917.1:n.-7+62423G=