Canonical Allele Identifier: CA10637456
Community Standard Title: NM_001025389.2(AMPD3):c.*1181dup
Gene: AMPD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10507065dup , CM000673.2:g.10507065dup GRCh38
NC_000011.9:g.10528612dup , CM000673.1:g.10528612dup GRCh37
NC_000011.8:g.10485188dup NCBI36
NG_012041.1:g.61389dup

Transcript Alleles

HGVS Amino-acid Change
NM_001025389.2:c.*1181dup MANE Select NP_001020560.1:n.*1181dup
ENST00000396553.7:c.*1181dup MANE Select ENSP00000379801.2:n.*1181dup
NM_000480.2:c.*1181dup NP_000471.1:n.*1181dup
NM_000480.3:c.*1181dup NP_000471.1:n.*1181dup
NM_001025389.1:c.*1181dup NP_001020560.1:n.*1181dup
NM_001025390.1:c.*1181dup NP_001020561.1:n.*1181dup
NM_001025390.2:c.*1181dup NP_001020561.1:n.*1181dup
NM_001172430.1:c.*1181dup NP_001165901.1:n.*1181dup
NM_001172431.1:c.*1181dup NP_001165902.1:n.*1181dup
NM_001172431.2:c.*1181dup NP_001165902.1:n.*1181dup
ENST00000396553.6:c.*1181dup ENSP00000379801.2:n.*1181dup
ENST00000444303.6:c.*1181dup ENSP00000396000.2:n.*1181dup