Canonical Allele Identifier: CA2802892566

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922680C>G , CM000676.2:g.102922680C>G	GRCh38
NC_000014.8:g.103389017C>G , CM000676.1:g.103389017C>G	GRCh37
NC_000014.7:g.102458770C>G	NCBI36
NG_008276.2:g.5025C>G , LRG_642:g.5025C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-9C>G MANE Select	ENSP00000299155.6:n.-9C>G
ENST00000299155.9:c.-9C>G	ENSP00000299155.5:n.-9C>G
NM_030943.3:c.-9C>G , LRG_642t1:c.-9C>G	NP_112205.2:n.-9C>G
XM_011537202.1:c.-190C>G	XP_011535504.1:n.-190C>G
XM_011537202.3:c.-190C>G	XP_011535504.1:n.-190C>G
XM_024449714.1:c.88C>G	XP_024305482.1:p.Arg30Gly
NM_030943.4:c.-9C>G MANE Select	NP_112205.2:n.-9C>G