Canonical Allele Identifier: CA2647247520
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677773_114677807del , CM000663.2:g.114677773_114677807del GRCh38
NC_000001.10:g.115220394_115220428del , CM000663.1:g.115220394_115220428del GRCh37
NC_000001.9:g.115021917_115021951del NCBI36
NG_008012.1:g.22749_22783del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1212+103_1212+137del ENSP00000358551.4:n.1212+103_1212+137del
ENST00000520113.7:c.1224+103_1224+137del MANE Select ENSP00000430075.3:n.1224+103_1224+137del
ENST00000637080.1:c.1007+103_1007+137del ENSP00000489753.1:n.1007+103_1007+137del
ENST00000639077.1:n.889+103_889+137del
ENST00000369538.3:c.1311+103_1311+137del ENSP00000358551.3:n.1311+103_1311+137del
ENST00000520113.6:c.1323+103_1323+137del ENSP00000430075.2:n.1323+103_1323+137del
NM_000036.2:c.1323+103_1323+137del NP_000027.2:n.1323+103_1323+137del
NM_001172626.1:c.1311+103_1311+137del NP_001166097.1:n.1311+103_1311+137del
NM_000036.3:c.1224+103_1224+137del MANE Select NP_000027.3:n.1224+103_1224+137del
NM_001172626.2:c.1212+103_1212+137del NP_001166097.2:n.1212+103_1212+137del