Canonical Allele Identifier: CA2160048488

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922665_102922677delinsTGGGGTGCAAGGA , CM000676.2:g.102922665_102922677delinsTGGGGTGCAAGGA	GRCh38
NC_000014.8:g.103389002_103389014delinsTGGGGTGCAAGGA , CM000676.1:g.103389002_103389014delinsTGGGGTGCAAGGA	GRCh37
NC_000014.7:g.102458755_102458767delinsTGGGGTGCAAGGA	NCBI36
NG_008276.2:g.5010_5022delinsTGGGGTGCAAGGA , LRG_642:g.5010_5022delinsTGGGGTGCAAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-24_-12delinsTGGGGTGCAAGGA MANE Select	ENSP00000299155.6:n.-24_-12delinsTGGGGTGCAAGGA
ENST00000299155.9:c.-24_-12delinsTGGGGTGCAAGGA	ENSP00000299155.5:n.-24_-12delinsTGGGGTGCAAGGA
NM_030943.3:c.-24_-12delinsTGGGGTGCAAGGA , LRG_642t1:c.-24_-12delinsTGGGGTGCAAGGA	NP_112205.2:n.-24_-12delinsTGGGGTGCAAGGA
XM_011537202.1:c.-205_-193delinsTGGGGTGCAAGGA	XP_011535504.1:n.-205_-193delinsTGGGGTGCAAGGA
XM_011537202.3:c.-205_-193delinsTGGGGTGCAAGGA	XP_011535504.1:n.-205_-193delinsTGGGGTGCAAGGA
XM_024449714.1:c.73_85delinsTGGGGTGCAAGGA	XP_024305482.1:p.Trp25=
NM_030943.4:c.-24_-12delinsTGGGGTGCAAGGA MANE Select	NP_112205.2:n.-24_-12delinsTGGGGTGCAAGGA