Canonical Allele Identifier: CA2802892567

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922702dup , CM000676.2:g.102922702dup	GRCh38
NC_000014.8:g.103389039dup , CM000676.1:g.103389039dup	GRCh37
NC_000014.7:g.102458792dup	NCBI36
NG_008276.2:g.5047dup , LRG_642:g.5047dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.14dup MANE Select	ENSP00000299155.6:p.Arg6ProfsTer?
ENST00000299155.9:c.14dup	ENSP00000299155.5:p.Arg6ProfsTer?
NM_030943.3:c.14dup , LRG_642t1:c.14dup	NP_112205.2:p.Arg6ProfsTer?
XM_011537202.1:c.-168dup	XP_011535504.1:n.-168dup
XM_011537202.3:c.-168dup	XP_011535504.1:n.-168dup
XM_024449714.1:c.110dup	XP_024305482.1:p.Arg38ProfsTer?
NM_030943.4:c.14dup MANE Select	NP_112205.2:p.Arg6ProfsTer?