Canonical Allele Identifier: CA2839254625
Gene: AMN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922744dup , CM000676.2:g.102922744dup GRCh38
NC_000014.8:g.103389081dup , CM000676.1:g.103389081dup GRCh37
NC_000014.7:g.102458834dup NCBI36
NG_008276.2:g.5089dup , LRG_642:g.5089dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.43+13dup MANE Select ENSP00000299155.6:n.43+13dup
ENST00000299155.9:c.43+13dup ENSP00000299155.5:n.43+13dup
NM_030943.3:c.43+13dup , LRG_642t1:c.43+13dup NP_112205.2:n.43+13dup
XM_011537202.1:c.-126dup XP_011535504.1:n.-126dup
XM_011537202.3:c.-126dup XP_011535504.1:n.-126dup
XM_024449714.1:c.139+13dup XP_024305482.1:n.139+13dup
NM_030943.4:c.43+13dup MANE Select NP_112205.2:n.43+13dup
Search 100 bp 5'
Search 100 bp 3'