Canonical Allele Identifier: CA2841429626

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922760dup , CM000676.2:g.102922760dup	GRCh38
NC_000014.8:g.103389097dup , CM000676.1:g.103389097dup	GRCh37
NC_000014.7:g.102458850dup	NCBI36
NG_008276.2:g.5105dup , LRG_642:g.5105dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.43+29dup MANE Select	ENSP00000299155.6:n.43+29dup
ENST00000299155.9:c.43+29dup	ENSP00000299155.5:n.43+29dup
NM_030943.3:c.43+29dup , LRG_642t1:c.43+29dup	NP_112205.2:n.43+29dup
XM_011537202.1:c.-120+10dup	XP_011535504.1:n.-120+10dup
XM_011537202.3:c.-120+10dup	XP_011535504.1:n.-120+10dup
XM_024449714.1:c.139+29dup	XP_024305482.1:n.139+29dup
NM_030943.4:c.43+29dup MANE Select	NP_112205.2:n.43+29dup