Canonical Allele Identifier: CA2575630671

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922681G>C , CM000676.2:g.102922681G>C	GRCh38
NC_000014.8:g.103389018G>C , CM000676.1:g.103389018G>C	GRCh37
NC_000014.7:g.102458771G>C	NCBI36
NG_008276.2:g.5026G>C , LRG_642:g.5026G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-8G>C MANE Select	ENSP00000299155.6:n.-8G>C
ENST00000299155.9:c.-8G>C	ENSP00000299155.5:n.-8G>C
NM_030943.3:c.-8G>C , LRG_642t1:c.-8G>C	NP_112205.2:n.-8G>C
XM_011537202.1:c.-189G>C	XP_011535504.1:n.-189G>C
XM_011537202.3:c.-189G>C	XP_011535504.1:n.-189G>C
XM_024449714.1:c.89G>C	XP_024305482.1:p.Arg30Pro
NM_030943.4:c.-8G>C MANE Select	NP_112205.2:n.-8G>C