Canonical Allele Identifier: CA2160048517

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922705G= , CM000676.2:g.102922705G=	GRCh38
NC_000014.8:g.103389042G= , CM000676.1:g.103389042G=	GRCh37
NC_000014.7:g.102458795G=	NCBI36
NG_008276.2:g.5050G= , LRG_642:g.5050G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.17G= MANE Select	ENSP00000299155.6:p.Arg6=
ENST00000299155.9:c.17G=	ENSP00000299155.5:p.Arg6=
NM_030943.3:c.17G= , LRG_642t1:c.17G=	NP_112205.2:p.Arg6=
XM_011537202.1:c.-165G=	XP_011535504.1:n.-165G=
XM_011537202.3:c.-165G=	XP_011535504.1:n.-165G=
XM_024449714.1:c.113G=	XP_024305482.1:p.Arg38=
NM_030943.4:c.17G= MANE Select	NP_112205.2:p.Arg6=