Canonical Allele Identifier: CA487995983
Gene: AMN HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.103389084del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922747del , CM000676.2:g.102922747del GRCh38
NC_000014.8:g.103389084del , CM000676.1:g.103389084del GRCh37
NC_000014.7:g.102458837del NCBI36
NG_008276.2:g.5092del , LRG_642:g.5092del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.43+16del MANE Select ENSP00000299155.6:n.43+16del
ENST00000299155.9:c.43+16del ENSP00000299155.5:n.43+16del
NM_030943.3:c.43+16del , LRG_642t1:c.43+16del NP_112205.2:n.43+16del
XM_011537202.1:c.-123del XP_011535504.1:n.-123del
XM_011537202.3:c.-123del XP_011535504.1:n.-123del
XM_024449714.1:c.139+16del XP_024305482.1:n.139+16del
NM_030943.4:c.43+16del MANE Select NP_112205.2:n.43+16del
Search 100 bp 5'
Search 100 bp 3'