Canonical Allele Identifier: CA1190277352
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114679579C= , CM000663.2:g.114679579C= GRCh38
NC_000001.10:g.115222200C= , CM000663.1:g.115222200C= GRCh37
NC_000001.9:g.115023723C= NCBI36
NG_008012.1:g.20977G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.885G= ENSP00000358551.4:p.Lys295=
ENST00000520113.7:c.897G= MANE Select ENSP00000430075.3:p.Lys299=
ENST00000637080.1:c.680G= ENSP00000489753.1:n.680G=
ENST00000639077.1:n.562G=
ENST00000369538.3:c.984G= ENSP00000358551.3:p.Lys328=
ENST00000520113.6:c.996G= ENSP00000430075.2:p.Lys332=
NM_000036.2:c.996G= NP_000027.2:p.Lys332=
NM_001172626.1:c.984G= NP_001166097.1:p.Lys328=
NM_000036.3:c.897G= MANE Select NP_000027.3:p.Lys299=
NM_001172626.2:c.885G= NP_001166097.2:p.Lys295=