Canonical Allele Identifier: CA2647247398
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677759_114677760insGGGGGG , CM000663.2:g.114677759_114677760insGGGGGG GRCh38
NC_000001.10:g.115220380_115220381insGGGGGG , CM000663.1:g.115220380_115220381insGGGGGG GRCh37
NC_000001.9:g.115021903_115021904insGGGGGG NCBI36
NG_008012.1:g.22796_22797insCCCCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1212+150_1212+151insCCCCCC ENSP00000358551.4:n.1212+150_1212+151insCCCCCC
ENST00000520113.7:c.1224+150_1224+151insCCCCCC MANE Select ENSP00000430075.3:n.1224+150_1224+151insCCCCCC
ENST00000637080.1:c.1007+150_1007+151insCCCCCC ENSP00000489753.1:n.1007+150_1007+151insCCCCCC
ENST00000639077.1:n.889+150_889+151insCCCCCC
ENST00000369538.3:c.1311+150_1311+151insCCCCCC ENSP00000358551.3:n.1311+150_1311+151insCCCCCC
ENST00000520113.6:c.1323+150_1323+151insCCCCCC ENSP00000430075.2:n.1323+150_1323+151insCCCCCC
NM_000036.2:c.1323+150_1323+151insCCCCCC NP_000027.2:n.1323+150_1323+151insCCCCCC
NM_001172626.1:c.1311+150_1311+151insCCCCCC NP_001166097.1:n.1311+150_1311+151insCCCCCC
NM_000036.3:c.1224+150_1224+151insCCCCCC MANE Select NP_000027.3:n.1224+150_1224+151insCCCCCC
NM_001172626.2:c.1212+150_1212+151insCCCCCC NP_001166097.2:n.1212+150_1212+151insCCCCCC