Canonical Allele Identifier: CA419883780
Gene: AMPD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115236067A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114693446A>T , CM000663.2:g.114693446A>T GRCh38
NC_000001.10:g.115236067A>T , CM000663.1:g.115236067A>T GRCh37
NC_000001.9:g.115037590A>T NCBI36
NG_008012.1:g.7110T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.22+2004T>A ENSP00000358551.4:n.22+2004T>A
ENST00000520113.7:c.24T>A MANE Select ENSP00000430075.3:p.Ala8=
ENST00000637080.1:c.37+1991T>A ENSP00000489753.1:n.37+1991T>A
ENST00000369538.3:c.121+2004T>A ENSP00000358551.3:n.121+2004T>A
ENST00000520113.6:c.123T>A ENSP00000430075.2:p.Ala41=
NM_000036.2:c.123T>A NP_000027.2:p.Ala41=
NM_001172626.1:c.121+2004T>A NP_001166097.1:n.121+2004T>A
NM_000036.3:c.24T>A MANE Select NP_000027.3:p.Ala8=
NM_001172626.2:c.22+2004T>A NP_001166097.2:n.22+2004T>A