Canonical Allele Identifier: CA15109580
Gene: DDAH1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.85379684T>C
GRCh37 chr1:g.85845367T>C
gnomAD v2:
1:85845367 T / C
gnomAD v3:
1:85379684 T / C
gnomAD v4:
chr1-85379684-T-C
Joint Max Group AF 0.40370425 (SAS)
Genomes Max Group AF 0.39091473 (SAS)
Exomes Max Group AF 0.40417291 (SAS)
dbSNP:
997251
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.85379684T>C , CM000663.2:g.85379684T>C GRCh38
NC_000001.10:g.85845367T>C , CM000663.1:g.85845367T>C GRCh37
NC_000001.9:g.85617955T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000284031.13:c.304-20837A>G MANE Select ENSP00000284031.8:n.304-20837A>G
ENST00000426972.8:c.-6-20837A>G ENSP00000411189.4:n.-6-20837A>G
ENST00000284031.12:c.304-20837A>G ENSP00000284031.8:n.304-20837A>G
ENST00000426972.7:c.-6-20837A>G ENSP00000411189.4:n.-6-20837A>G
ENST00000483110.5:n.384-20837A>G
ENST00000535924.6:c.-6-20837A>G ENSP00000439045.1:n.-6-20837A>G
ENST00000539042.3:c.304-20837A>G ENSP00000438604.1:n.304-20837A>G
ENST00000633113.1:c.4-20837A>G ENSP00000488725.1:n.4-20837A>G
NM_001134445.1:c.-6-20837A>G NP_001127917.1:n.-6-20837A>G
NM_012137.3:c.304-20837A>G NP_036269.1:n.304-20837A>G
XM_005270707.2:c.19-20837A>G XP_005270764.1:n.19-20837A>G
XM_005270709.2:c.-6-20837A>G XP_005270766.1:n.-6-20837A>G
XM_005270710.2:c.-110A>G XP_005270767.1:n.-110A>G
XM_006710544.1:c.-7+104A>G XP_006710607.1:n.-7+104A>G
XM_011541158.1:c.-86-19147A>G XP_011539460.1:n.-86-19147A>G
NM_001330655.1:c.4-20837A>G NP_001317584.1:n.4-20837A>G
XM_017000889.1:c.25-20837A>G XP_016856378.1:n.25-20837A>G
XM_024446130.1:c.-6-20837A>G XP_024301898.1:n.-6-20837A>G
NM_012137.4:c.304-20837A>G MANE Select NP_036269.1:n.304-20837A>G
NM_001134445.2:c.-6-20837A>G NP_001127917.1:n.-6-20837A>G
NM_001330655.2:c.4-20837A>G NP_001317584.1:n.4-20837A>G
Search 100 bp 5'
Search 100 bp 3'