Canonical Allele Identifier: CA10980511

Gene: DDAH1

Linked Data

• dbSNP Id: rs1554597
• gnomAD v2: 1-85877098-C-T
• gnomAD v3: 1-85411415-C-T
• gnomAD v4: 1-85411415-C-T
• MyVariant Identifiers: chr1:g.85877098C>T (hg19) ; chr1:g.85411415C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85411415C>T , CM000663.2:g.85411415C>T	GRCh38
NC_000001.10:g.85877098C>T , CM000663.1:g.85877098C>T	GRCh37
NC_000001.9:g.85649686C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000284031.13:c.304-52568G>A MANE Select	ENSP00000284031.8:n.304-52568G>A
ENST00000426972.8:c.-6-52568G>A	ENSP00000411189.4:n.-6-52568G>A
ENST00000284031.12:c.304-52568G>A	ENSP00000284031.8:n.304-52568G>A
ENST00000426972.7:c.-6-52568G>A	ENSP00000411189.4:n.-6-52568G>A
ENST00000483110.5:n.384-52568G>A
ENST00000535924.6:c.-6-52568G>A	ENSP00000439045.1:n.-6-52568G>A
ENST00000539042.3:c.304-52568G>A	ENSP00000438604.1:n.304-52568G>A
NM_001134445.1:c.-6-52568G>A	NP_001127917.1:n.-6-52568G>A
NM_012137.3:c.304-52568G>A	NP_036269.1:n.304-52568G>A
XM_005270707.2:c.19-52568G>A	XP_005270764.1:n.19-52568G>A
XM_005270709.2:c.-6-52568G>A	XP_005270766.1:n.-6-52568G>A
XM_011541158.1:c.-86-50878G>A	XP_011539460.1:n.-86-50878G>A
XM_017000889.1:c.25-52568G>A	XP_016856378.1:n.25-52568G>A
XM_024446130.1:c.-6-52568G>A	XP_024301898.1:n.-6-52568G>A
NM_012137.4:c.304-52568G>A MANE Select	NP_036269.1:n.304-52568G>A
NM_001134445.2:c.-6-52568G>A	NP_001127917.1:n.-6-52568G>A