Canonical Allele Identifier: CA2647249051
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114679463C>A , CM000663.2:g.114679463C>A GRCh38
NC_000001.10:g.115222084C>A , CM000663.1:g.115222084C>A GRCh37
NC_000001.9:g.115023607C>A NCBI36
NG_008012.1:g.21093G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.885+116G>T ENSP00000358551.4:n.885+116G>T
ENST00000520113.7:c.897+116G>T MANE Select ENSP00000430075.3:n.897+116G>T
ENST00000637080.1:c.680+116G>T ENSP00000489753.1:n.680+116G>T
ENST00000639077.1:n.562+116G>T
ENST00000369538.3:c.984+116G>T ENSP00000358551.3:n.984+116G>T
ENST00000520113.6:c.996+116G>T ENSP00000430075.2:n.996+116G>T
NM_000036.2:c.996+116G>T NP_000027.2:n.996+116G>T
NM_001172626.1:c.984+116G>T NP_001166097.1:n.984+116G>T
NM_000036.3:c.897+116G>T MANE Select NP_000027.3:n.897+116G>T
NM_001172626.2:c.885+116G>T NP_001166097.2:n.885+116G>T