Canonical Allele Identifier: CA1143782254
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684295T= , CM000663.2:g.114684295T= GRCh38
NC_000001.10:g.115226916T= , CM000663.1:g.115226916T= GRCh37
NC_000001.9:g.115028439T= NCBI36
NG_008012.1:g.16261A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.439A= ENSP00000358551.4:p.Met147=
ENST00000520113.7:c.451A= MANE Select ENSP00000430075.3:p.Met151=
ENST00000637080.1:c.454A= ENSP00000489753.1:p.Met152=
ENST00000639077.1:n.116A=
ENST00000369538.3:c.538A= ENSP00000358551.3:p.Met180=
ENST00000485564.3:n.325A=
ENST00000520113.6:c.550A= ENSP00000430075.2:p.Met184=
NM_000036.2:c.550A= NP_000027.2:p.Met184=
NM_001172626.1:c.538A= NP_001166097.1:p.Met180=
NM_000036.3:c.451A= MANE Select NP_000027.3:p.Met151=
NM_001172626.2:c.439A= NP_001166097.2:p.Met147=