Canonical Allele Identifier: CA2647248006
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677830_114677831insGTCC , CM000663.2:g.114677830_114677831insGTCC GRCh38
NC_000001.10:g.115220451_115220452insGTCC , CM000663.1:g.115220451_115220452insGTCC GRCh37
NC_000001.9:g.115021974_115021975insGTCC NCBI36
NG_008012.1:g.22728_22729insCGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1212+82_1212+83insCGGA ENSP00000358551.4:n.1212+82_1212+83insCGGA
ENST00000520113.7:c.1224+82_1224+83insCGGA MANE Select ENSP00000430075.3:n.1224+82_1224+83insCGGA
ENST00000637080.1:c.1007+82_1007+83insCGGA ENSP00000489753.1:n.1007+82_1007+83insCGGA
ENST00000639077.1:n.889+82_889+83insCGGA
ENST00000369538.3:c.1311+82_1311+83insCGGA ENSP00000358551.3:n.1311+82_1311+83insCGGA
ENST00000520113.6:c.1323+82_1323+83insCGGA ENSP00000430075.2:n.1323+82_1323+83insCGGA
NM_000036.2:c.1323+82_1323+83insCGGA NP_000027.2:n.1323+82_1323+83insCGGA
NM_001172626.1:c.1311+82_1311+83insCGGA NP_001166097.1:n.1311+82_1311+83insCGGA
NM_000036.3:c.1224+82_1224+83insCGGA MANE Select NP_000027.3:n.1224+82_1224+83insCGGA
NM_001172626.2:c.1212+82_1212+83insCGGA NP_001166097.2:n.1212+82_1212+83insCGGA