Canonical Allele Identifier: CA2160048561

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922769G= , CM000676.2:g.102922769G=	GRCh38
NC_000014.8:g.103389106G= , CM000676.1:g.103389106G=	GRCh37
NC_000014.7:g.102458859G=	NCBI36
NG_008276.2:g.5114G= , LRG_642:g.5114G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.43+38G= MANE Select	ENSP00000299155.6:n.43+38G=
ENST00000299155.9:c.43+38G=	ENSP00000299155.5:n.43+38G=
NM_030943.3:c.43+38G= , LRG_642t1:c.43+38G=	NP_112205.2:n.43+38G=
XM_011537202.1:c.-120+19G=	XP_011535504.1:n.-120+19G=
XM_011537202.3:c.-120+19G=	XP_011535504.1:n.-120+19G=
XM_024449714.1:c.139+38G=	XP_024305482.1:n.139+38G=
NM_030943.4:c.43+38G= MANE Select	NP_112205.2:n.43+38G=