Canonical Allele Identifier: CA2160048495

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922674A= , CM000676.2:g.102922674A=	GRCh38
NC_000014.8:g.103389011A= , CM000676.1:g.103389011A=	GRCh37
NC_000014.7:g.102458764A=	NCBI36
NG_008276.2:g.5019A= , LRG_642:g.5019A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-15A= MANE Select	ENSP00000299155.6:n.-15A=
ENST00000299155.9:c.-15A=	ENSP00000299155.5:n.-15A=
NM_030943.3:c.-15A= , LRG_642t1:c.-15A=	NP_112205.2:n.-15A=
XM_011537202.1:c.-196A=	XP_011535504.1:n.-196A=
XM_011537202.3:c.-196A=	XP_011535504.1:n.-196A=
XM_024449714.1:c.82A=	XP_024305482.1:p.Arg28=
NM_030943.4:c.-15A= MANE Select	NP_112205.2:n.-15A=