Canonical Allele Identifier: CA2160048492

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922669_102922672delinsGTGC , CM000676.2:g.102922669_102922672delinsGTGC	GRCh38
NC_000014.8:g.103389006_103389009delinsGTGC , CM000676.1:g.103389006_103389009delinsGTGC	GRCh37
NC_000014.7:g.102458759_102458762delinsGTGC	NCBI36
NG_008276.2:g.5014_5017delinsGTGC , LRG_642:g.5014_5017delinsGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-20_-17delinsGTGC MANE Select	ENSP00000299155.6:n.-20_-17delinsGTGC
ENST00000299155.9:c.-20_-17delinsGTGC	ENSP00000299155.5:n.-20_-17delinsGTGC
NM_030943.3:c.-20_-17delinsGTGC , LRG_642t1:c.-20_-17delinsGTGC	NP_112205.2:n.-20_-17delinsGTGC
XM_011537202.1:c.-201_-198delinsGTGC	XP_011535504.1:n.-201_-198delinsGTGC
XM_011537202.3:c.-201_-198delinsGTGC	XP_011535504.1:n.-201_-198delinsGTGC
XM_024449714.1:c.77_80delinsGTGC	XP_024305482.1:p.Gly26=
NM_030943.4:c.-20_-17delinsGTGC MANE Select	NP_112205.2:n.-20_-17delinsGTGC