Canonical Allele Identifier: CA2476076580
Gene: DDAH1 HGNC NCBI

Linked Data

dbSNP Id: rs1557625247

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.85433794A>T , CM000663.2:g.85433794A>T GRCh38
NC_000001.10:g.85899477A>T , CM000663.1:g.85899477A>T GRCh37
NC_000001.9:g.85672065A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000284031.13:c.303+30949T>A MANE Select ENSP00000284031.8:n.303+30949T>A
ENST00000426972.8:c.-7+62372T>A ENSP00000411189.4:n.-7+62372T>A
ENST00000284031.12:c.303+30949T>A ENSP00000284031.8:n.303+30949T>A
ENST00000426972.7:c.-7+62372T>A ENSP00000411189.4:n.-7+62372T>A
ENST00000483110.5:n.383+62372T>A
ENST00000535924.6:c.-7+62372T>A ENSP00000439045.1:n.-7+62372T>A
ENST00000539042.3:c.303+30949T>A ENSP00000438604.1:n.303+30949T>A
NM_001134445.1:c.-7+62372T>A NP_001127917.1:n.-7+62372T>A
NM_012137.3:c.303+30949T>A NP_036269.1:n.303+30949T>A
XM_005270707.2:c.19-74947T>A XP_005270764.1:n.19-74947T>A
XM_005270709.2:c.-7+62372T>A XP_005270766.1:n.-7+62372T>A
XM_011541158.1:c.-87+62372T>A XP_011539460.1:n.-87+62372T>A
XM_017000889.1:c.24+30702T>A XP_016856378.1:n.24+30702T>A
XM_024446130.1:c.-7+62372T>A XP_024301898.1:n.-7+62372T>A
NM_012137.4:c.303+30949T>A MANE Select NP_036269.1:n.303+30949T>A
NM_001134445.2:c.-7+62372T>A NP_001127917.1:n.-7+62372T>A