Canonical Allele Identifier: CA419883776
Gene: AMPD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115236058T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114693437T>C , CM000663.2:g.114693437T>C GRCh38
NC_000001.10:g.115236058T>C , CM000663.1:g.115236058T>C GRCh37
NC_000001.9:g.115037581T>C NCBI36
NG_008012.1:g.7119A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.22+2013A>G ENSP00000358551.4:n.22+2013A>G
ENST00000520113.7:c.33A>G MANE Select ENSP00000430075.3:p.Lys11=
ENST00000637080.1:c.37+2000A>G ENSP00000489753.1:n.37+2000A>G
ENST00000369538.3:c.121+2013A>G ENSP00000358551.3:n.121+2013A>G
ENST00000520113.6:c.132A>G ENSP00000430075.2:p.Lys44=
NM_000036.2:c.132A>G NP_000027.2:p.Lys44=
NM_001172626.1:c.121+2013A>G NP_001166097.1:n.121+2013A>G
NM_000036.3:c.33A>G MANE Select NP_000027.3:p.Lys11=
NM_001172626.2:c.22+2013A>G NP_001166097.2:n.22+2013A>G