Canonical Allele Identifier: CA2160048486

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922665T= , CM000676.2:g.102922665T=	GRCh38
NC_000014.8:g.103389002T= , CM000676.1:g.103389002T=	GRCh37
NC_000014.7:g.102458755T=	NCBI36
NG_008276.2:g.5010T= , LRG_642:g.5010T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-24T= MANE Select	ENSP00000299155.6:n.-24T=
ENST00000299155.9:c.-24T=	ENSP00000299155.5:n.-24T=
NM_030943.3:c.-24T= , LRG_642t1:c.-24T=	NP_112205.2:n.-24T=
XM_011537202.1:c.-205T=	XP_011535504.1:n.-205T=
XM_011537202.3:c.-205T=	XP_011535504.1:n.-205T=
XM_024449714.1:c.73T=	XP_024305482.1:p.Trp25=
NM_030943.4:c.-24T= MANE Select	NP_112205.2:n.-24T=