Canonical Allele Identifier: CA2160048477

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922652_102922654delinsCAA , CM000676.2:g.102922652_102922654delinsCAA	GRCh38
NC_000014.8:g.103388989_103388991delinsCAA , CM000676.1:g.103388989_103388991delinsCAA	GRCh37
NC_000014.7:g.102458742_102458744delinsCAA	NCBI36
NG_008276.2:g.4997_4999delinsCAA , LRG_642:g.4997_4999delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
XM_011537202.1:c.-218_-216delinsCAA	XP_011535504.1:n.-218_-216delinsCAA
XM_011537202.3:c.-218_-216delinsCAA	XP_011535504.1:n.-218_-216delinsCAA
XM_024449714.1:c.60_62delinsCAA	XP_024305482.1:p.Gly20=