Canonical Allele Identifier: CA1190282051
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684401_114684402delinsTC , CM000663.2:g.114684401_114684402delinsTC GRCh38
NC_000001.10:g.115227022_115227023delinsTC , CM000663.1:g.115227022_115227023delinsTC GRCh37
NC_000001.9:g.115028545_115028546delinsTC NCBI36
NG_008012.1:g.16154_16155delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.370-38_370-37delinsGA ENSP00000358551.4:n.370-38_370-37delinsGA
ENST00000520113.7:c.382-38_382-37delinsGA MANE Select ENSP00000430075.3:n.382-38_382-37delinsGA
ENST00000637080.1:c.385-38_385-37delinsGA ENSP00000489753.1:n.385-38_385-37delinsGA
ENST00000639077.1:n.47-38_47-37delinsGA
ENST00000369538.3:c.469-38_469-37delinsGA ENSP00000358551.3:n.469-38_469-37delinsGA
ENST00000485564.3:n.256-38_256-37delinsGA
ENST00000520113.6:c.481-38_481-37delinsGA ENSP00000430075.2:n.481-38_481-37delinsGA
NM_000036.2:c.481-38_481-37delinsGA NP_000027.2:n.481-38_481-37delinsGA
NM_001172626.1:c.469-38_469-37delinsGA NP_001166097.1:n.469-38_469-37delinsGA
NM_000036.3:c.382-38_382-37delinsGA MANE Select NP_000027.3:n.382-38_382-37delinsGA
NM_001172626.2:c.370-38_370-37delinsGA NP_001166097.2:n.370-38_370-37delinsGA