Canonical Allele Identifier: CA645574466
Gene: AMN HGNC NCBI

Linked Data

COSMIC: COSM6458829
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922701_102922702insAT , CM000676.2:g.102922701_102922702insAT GRCh38
NC_000014.8:g.103389038_103389039insAT , CM000676.1:g.103389038_103389039insAT GRCh37
NC_000014.7:g.102458791_102458792insAT NCBI36
NG_008276.2:g.5046_5047insAT , LRG_642:g.5046_5047insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.13_14insAT MANE Select ENSP00000299155.6:p.Gly5AspfsTer13
ENST00000299155.9:c.13_14insAT ENSP00000299155.5:p.Gly5AspfsTer13
NM_030943.3:c.13_14insAT , LRG_642t1:c.13_14insAT NP_112205.2:p.Gly5AspfsTer13
XM_011537202.1:c.-169_-168insAT XP_011535504.1:n.-169_-168insAT
XM_011537202.3:c.-169_-168insAT XP_011535504.1:n.-169_-168insAT
XM_024449714.1:c.109_110insAT XP_024305482.1:p.Gly37AspfsTer13
NM_030943.4:c.13_14insAT MANE Select NP_112205.2:p.Gly5AspfsTer13
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