Canonical Allele Identifier: CA25649180

Gene: DDAH1

Linked Data

• dbSNP Id: rs972328787
• gnomAD v3: 1-85321213-T-C
• gnomAD v4: 1-85321213-T-C
• MyVariant Identifiers: chr1:g.85786896T>C (hg19) ; chr1:g.85321213T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85321213T>C , CM000663.2:g.85321213T>C	GRCh38
NC_000001.10:g.85786896T>C , CM000663.1:g.85786896T>C	GRCh37
NC_000001.9:g.85559484T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284031.13:c.*239A>G MANE Select	ENSP00000284031.8:n.*239A>G
ENST00000426972.8:c.*239A>G	ENSP00000411189.4:n.*239A>G
ENST00000284031.12:c.*239A>G	ENSP00000284031.8:n.*239A>G
ENST00000426972.7:c.*239A>G	ENSP00000411189.4:n.*239A>G
ENST00000483110.5:n.1177A>G
ENST00000535924.6:c.*239A>G	ENSP00000439045.1:n.*239A>G
ENST00000539042.3:c.*150+89A>G	ENSP00000438604.1:n.*150+89A>G
NM_001134445.1:c.*239A>G	NP_001127917.1:n.*239A>G
NM_012137.3:c.*239A>G	NP_036269.1:n.*239A>G
XM_005270707.2:c.*239A>G	XP_005270764.1:n.*239A>G
XM_005270709.2:c.*239A>G	XP_005270766.1:n.*239A>G
XM_005270710.2:c.*239A>G	XP_005270767.1:n.*239A>G
XM_006710544.1:c.*239A>G	XP_006710607.1:n.*239A>G
XM_011541158.1:c.*239A>G	XP_011539460.1:n.*239A>G
NM_001330655.1:c.*239A>G	NP_001317584.1:n.*239A>G
XM_017000889.1:c.*239A>G	XP_016856378.1:n.*239A>G
XM_024446130.1:c.*239A>G	XP_024301898.1:n.*239A>G
NM_012137.4:c.*239A>G MANE Select	NP_036269.1:n.*239A>G
NM_001134445.2:c.*239A>G	NP_001127917.1:n.*239A>G
NM_001330655.2:c.*239A>G	NP_001317584.1:n.*239A>G