Canonical Allele Identifier: CA15111589
Gene: DDAH1 HGNC NCBI

Linked Data

dbSNP Id: rs669173
gnomAD v2: 1-85899428-T-C
gnomAD v3: 1-85433745-T-C
gnomAD v4: 1-85433745-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.85433745T>C , CM000663.2:g.85433745T>C GRCh38
NC_000001.10:g.85899428T>C , CM000663.1:g.85899428T>C GRCh37
NC_000001.9:g.85672016T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000284031.13:c.303+30998A>G MANE Select ENSP00000284031.8:n.303+30998A>G
ENST00000426972.8:c.-7+62421A>G ENSP00000411189.4:n.-7+62421A>G
ENST00000284031.12:c.303+30998A>G ENSP00000284031.8:n.303+30998A>G
ENST00000426972.7:c.-7+62421A>G ENSP00000411189.4:n.-7+62421A>G
ENST00000483110.5:n.383+62421A>G
ENST00000535924.6:c.-7+62421A>G ENSP00000439045.1:n.-7+62421A>G
ENST00000539042.3:c.303+30998A>G ENSP00000438604.1:n.303+30998A>G
NM_001134445.1:c.-7+62421A>G NP_001127917.1:n.-7+62421A>G
NM_012137.3:c.303+30998A>G NP_036269.1:n.303+30998A>G
XM_005270707.2:c.19-74898A>G XP_005270764.1:n.19-74898A>G
XM_005270709.2:c.-7+62421A>G XP_005270766.1:n.-7+62421A>G
XM_011541158.1:c.-87+62421A>G XP_011539460.1:n.-87+62421A>G
XM_017000889.1:c.24+30751A>G XP_016856378.1:n.24+30751A>G
XM_024446130.1:c.-7+62421A>G XP_024301898.1:n.-7+62421A>G
NM_012137.4:c.303+30998A>G MANE Select NP_036269.1:n.303+30998A>G
NM_001134445.2:c.-7+62421A>G NP_001127917.1:n.-7+62421A>G