Canonical Allele Identifier: CA2160051555

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102928339T= , CM000676.2:g.102928339T=	GRCh38
NC_000014.8:g.103394676T= , CM000676.1:g.103394676T=	GRCh37
NC_000014.7:g.102464429T=	NCBI36
NG_008276.2:g.10684T= , LRG_642:g.10684T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299155.10:c.208-87T= MANE Select	ENSP00000299155.6:n.208-87T=
ENST00000299155.9:c.208-87T=	ENSP00000299155.5:n.208-87T=
ENST00000541086.5:n.954-87T=
NM_030943.3:c.208-87T= , LRG_642t1:c.208-87T=	NP_112205.2:n.208-87T=
XM_011537202.1:c.46-87T=	XP_011535504.1:n.46-87T=
XM_011537203.1:c.46-87T=	XP_011535505.1:n.46-87T=
XM_011537202.3:c.46-87T=	XP_011535504.1:n.46-87T=
XM_011537203.3:c.46-87T=	XP_011535505.1:n.46-87T=
XM_024449714.1:c.304-87T=	XP_024305482.1:n.304-87T=
NM_030943.4:c.208-87T= MANE Select	NP_112205.2:n.208-87T=