Canonical Allele Identifier: CA2802892791
Gene: AMN HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102928327del , CM000676.2:g.102928327del GRCh38
NC_000014.8:g.103394664del , CM000676.1:g.103394664del GRCh37
NC_000014.7:g.102464417del NCBI36
NG_008276.2:g.10672del , LRG_642:g.10672del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.208-99del MANE Select ENSP00000299155.6:n.208-99del
ENST00000299155.9:c.208-99del ENSP00000299155.5:n.208-99del
ENST00000541086.5:n.954-99del
NM_030943.3:c.208-99del , LRG_642t1:c.208-99del NP_112205.2:n.208-99del
XM_011537202.1:c.46-99del XP_011535504.1:n.46-99del
XM_011537203.1:c.46-99del XP_011535505.1:n.46-99del
XM_011537202.3:c.46-99del XP_011535504.1:n.46-99del
XM_011537203.3:c.46-99del XP_011535505.1:n.46-99del
XM_024449714.1:c.304-99del XP_024305482.1:n.304-99del
NM_030943.4:c.208-99del MANE Select NP_112205.2:n.208-99del
Search 100 bp 5'
Search 100 bp 3'