Canonical Allele Identifier: CA5882966

Gene: AMPD3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.10495557C>A , CM000673.2:g.10495557C>A	GRCh38
NC_000011.9:g.10517104C>A , CM000673.1:g.10517104C>A	GRCh37
NC_000011.8:g.10473680C>A	NCBI36
NG_012041.1:g.49881C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001025389.2:c.1267-13C>A MANE Select	NP_001020560.1:n.1267-13C>A
ENST00000396553.7:c.1267-13C>A MANE Select	ENSP00000379801.2:n.1267-13C>A
NM_000480.2:c.1294-13C>A	NP_000471.1:n.1294-13C>A
NM_000480.3:c.1294-13C>A	NP_000471.1:n.1294-13C>A
NM_001025389.1:c.1267-13C>A	NP_001020560.1:n.1267-13C>A
NM_001025390.1:c.1288-13C>A	NP_001020561.1:n.1288-13C>A
NM_001025390.2:c.1288-13C>A	NP_001020561.1:n.1288-13C>A
NM_001172430.1:c.1267-13C>A	NP_001165901.1:n.1267-13C>A
NM_001172431.1:c.790-13C>A	NP_001165902.1:n.790-13C>A
NM_001172431.2:c.790-13C>A	NP_001165902.1:n.790-13C>A
ENST00000396553.6:c.1267-13C>A	ENSP00000379801.2:n.1267-13C>A
ENST00000396554.7:c.1294-13C>A	ENSP00000379802.3:n.1294-13C>A
ENST00000444303.6:c.790-13C>A	ENSP00000396000.2:n.790-13C>A
ENST00000528723.5:c.1288-13C>A	ENSP00000436987.1:n.1288-13C>A
ENST00000529507.5:c.1267-13C>A	ENSP00000431648.1:n.1267-13C>A
ENST00000529834.5:c.1267-13C>A	ENSP00000435382.1:n.1267-13C>A
ENST00000533116.1:c.469-13C>A	ENSP00000433351.1:n.469-13C>A
ENST00000534047.5:c.*569-13C>A	ENSP00000433937.1:n.*569-13C>A