Canonical Allele Identifier: CA2160048506

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922689A= , CM000676.2:g.102922689A=	GRCh38
NC_000014.8:g.103389026A= , CM000676.1:g.103389026A=	GRCh37
NC_000014.7:g.102458779A=	NCBI36
NG_008276.2:g.5034A= , LRG_642:g.5034A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.1A= MANE Select	ENSP00000299155.6:p.Met1=
ENST00000299155.9:c.1A=	ENSP00000299155.5:p.Met1=
NM_030943.3:c.1A= , LRG_642t1:c.1A=	NP_112205.2:p.Met1=
XM_011537202.1:c.-181A=	XP_011535504.1:n.-181A=
XM_011537202.3:c.-181A=	XP_011535504.1:n.-181A=
XM_024449714.1:c.97A=	XP_024305482.1:p.Met33=
NM_030943.4:c.1A= MANE Select	NP_112205.2:p.Met1=