Canonical Allele Identifier: CA2574035256
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684418A>G , CM000663.2:g.114684418A>G GRCh38
NC_000001.10:g.115227039A>G , CM000663.1:g.115227039A>G GRCh37
NC_000001.9:g.115028562A>G NCBI36
NG_008012.1:g.16138T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.370-54T>C ENSP00000358551.4:n.370-54T>C
ENST00000520113.7:c.382-54T>C MANE Select ENSP00000430075.3:n.382-54T>C
ENST00000637080.1:c.385-54T>C ENSP00000489753.1:n.385-54T>C
ENST00000639077.1:n.46+26T>C
ENST00000369538.3:c.469-54T>C ENSP00000358551.3:n.469-54T>C
ENST00000485564.3:n.256-54T>C
ENST00000520113.6:c.481-54T>C ENSP00000430075.2:n.481-54T>C
NM_000036.2:c.481-54T>C NP_000027.2:n.481-54T>C
NM_001172626.1:c.469-54T>C NP_001166097.1:n.469-54T>C
NM_000036.3:c.382-54T>C MANE Select NP_000027.3:n.382-54T>C
NM_001172626.2:c.370-54T>C NP_001166097.2:n.370-54T>C