Canonical Allele Identifier: CA1190276618
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677986C= , CM000663.2:g.114677986C= GRCh38
NC_000001.10:g.115220607C= , CM000663.1:g.115220607C= GRCh37
NC_000001.9:g.115022130C= NCBI36
NG_008012.1:g.22570G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1136G= ENSP00000358551.4:p.Gly379=
ENST00000520113.7:c.1148G= MANE Select ENSP00000430075.3:p.Gly383=
ENST00000637080.1:n.931G= ENSP00000489753.1:n.931G=
ENST00000639077.1:n.813G=
ENST00000369538.3:c.1235G= ENSP00000358551.3:p.Gly412=
ENST00000520113.6:c.1247G= ENSP00000430075.2:p.Gly416=
NM_000036.2:c.1247G= NP_000027.2:p.Gly416=
NM_001172626.1:c.1235G= NP_001166097.1:p.Gly412=
NM_000036.3:c.1148G= MANE Select NP_000027.3:p.Gly383=
NM_001172626.2:c.1136G= NP_001166097.2:p.Gly379=