Canonical Allele Identifier: CA1141634653
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677405C= , CM000663.2:g.114677405C= GRCh38
NC_000001.10:g.115220026C= , CM000663.1:g.115220026C= GRCh37
NC_000001.9:g.115021549C= NCBI36
NG_008012.1:g.23151G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1322G= ENSP00000358551.4:p.Cys441=
ENST00000520113.7:c.1334G= MANE Select ENSP00000430075.3:p.Cys445=
ENST00000637080.1:c.1117G= ENSP00000489753.1:n.1117G=
ENST00000639077.1:n.999G=
ENST00000369538.3:c.1421G= ENSP00000358551.3:p.Cys474=
ENST00000520113.6:c.1433G= ENSP00000430075.2:p.Cys478=
NM_000036.2:c.1433G= NP_000027.2:p.Cys478=
NM_001172626.1:c.1421G= NP_001166097.1:p.Cys474=
NM_000036.3:c.1334G= MANE Select NP_000027.3:p.Cys445=
NM_001172626.2:c.1322G= NP_001166097.2:p.Cys441=