Canonical Allele Identifier: CA2160048494

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922672C= , CM000676.2:g.102922672C=	GRCh38
NC_000014.8:g.103389009C= , CM000676.1:g.103389009C=	GRCh37
NC_000014.7:g.102458762C=	NCBI36
NG_008276.2:g.5017C= , LRG_642:g.5017C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-17C= MANE Select	ENSP00000299155.6:n.-17C=
ENST00000299155.9:c.-17C=	ENSP00000299155.5:n.-17C=
NM_030943.3:c.-17C= , LRG_642t1:c.-17C=	NP_112205.2:n.-17C=
XM_011537202.1:c.-198C=	XP_011535504.1:n.-198C=
XM_011537202.3:c.-198C=	XP_011535504.1:n.-198C=
XM_024449714.1:c.80C=	XP_024305482.1:p.Ala27=
NM_030943.4:c.-17C= MANE Select	NP_112205.2:n.-17C=