Canonical Allele Identifier: CA341749148
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114678004T>A , CM000663.2:g.114678004T>A GRCh38
NC_000001.10:g.115220625T>A , CM000663.1:g.115220625T>A GRCh37
NC_000001.9:g.115022148T>A NCBI36
NG_008012.1:g.22552A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1118A>T ENSP00000358551.4:p.Asp373Val
ENST00000520113.7:c.1130A>T MANE Select ENSP00000430075.3:p.Asp377Val
ENST00000637080.1:c.913A>T ENSP00000489753.1:n.913A>T
ENST00000639077.1:n.795A>T
ENST00000369538.3:c.1217A>T ENSP00000358551.3:p.Asp406Val
ENST00000520113.6:c.1229A>T ENSP00000430075.2:p.Asp410Val
NM_000036.2:c.1229A>T NP_000027.2:p.Asp410Val
NM_001172626.1:c.1217A>T NP_001166097.1:p.Asp406Val
NM_000036.3:c.1130A>T MANE Select NP_000027.3:p.Asp377Val
NM_001172626.2:c.1118A>T NP_001166097.2:p.Asp373Val