Canonical Allele Identifier: CA1190276319
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677497C= , CM000663.2:g.114677497C= GRCh38
NC_000001.10:g.115220118C= , CM000663.1:g.115220118C= GRCh37
NC_000001.9:g.115021641C= NCBI36
NG_008012.1:g.23059G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1230G= ENSP00000358551.4:p.Leu410=
ENST00000520113.7:c.1242G= MANE Select ENSP00000430075.3:p.Leu414=
ENST00000637080.1:c.1025G= ENSP00000489753.1:n.1025G=
ENST00000639077.1:n.907G=
ENST00000369538.3:c.1329G= ENSP00000358551.3:p.Leu443=
ENST00000520113.6:c.1341G= ENSP00000430075.2:p.Leu447=
NM_000036.2:c.1341G= NP_000027.2:p.Leu447=
NM_001172626.1:c.1329G= NP_001166097.1:p.Leu443=
NM_000036.3:c.1242G= MANE Select NP_000027.3:p.Leu414=
NM_001172626.2:c.1230G= NP_001166097.2:p.Leu410=