Canonical Allele Identifier: CA419883778
Gene: AMPD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115236064T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114693443T>C , CM000663.2:g.114693443T>C GRCh38
NC_000001.10:g.115236064T>C , CM000663.1:g.115236064T>C GRCh37
NC_000001.9:g.115037587T>C NCBI36
NG_008012.1:g.7113A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.22+2007A>G ENSP00000358551.4:n.22+2007A>G
ENST00000520113.7:c.27A>G MANE Select ENSP00000430075.3:p.Glu9=
ENST00000637080.1:c.37+1994A>G ENSP00000489753.1:n.37+1994A>G
ENST00000369538.3:c.121+2007A>G ENSP00000358551.3:n.121+2007A>G
ENST00000520113.6:c.126A>G ENSP00000430075.2:p.Glu42=
NM_000036.2:c.126A>G NP_000027.2:p.Glu42=
NM_001172626.1:c.121+2007A>G NP_001166097.1:n.121+2007A>G
NM_000036.3:c.27A>G MANE Select NP_000027.3:p.Glu9=
NM_001172626.2:c.22+2007A>G NP_001166097.2:n.22+2007A>G