Canonical Allele Identifier: CA2647253810
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684390A>G , CM000663.2:g.114684390A>G GRCh38
NC_000001.10:g.115227011A>G , CM000663.1:g.115227011A>G GRCh37
NC_000001.9:g.115028534A>G NCBI36
NG_008012.1:g.16166T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.370-26T>C ENSP00000358551.4:n.370-26T>C
ENST00000520113.7:c.382-26T>C MANE Select ENSP00000430075.3:n.382-26T>C
ENST00000637080.1:c.385-26T>C ENSP00000489753.1:n.385-26T>C
ENST00000639077.1:n.47-26T>C
ENST00000369538.3:c.469-26T>C ENSP00000358551.3:n.469-26T>C
ENST00000485564.3:n.256-26T>C
ENST00000520113.6:c.481-26T>C ENSP00000430075.2:n.481-26T>C
NM_000036.2:c.481-26T>C NP_000027.2:n.481-26T>C
NM_001172626.1:c.469-26T>C NP_001166097.1:n.469-26T>C
NM_000036.3:c.382-26T>C MANE Select NP_000027.3:n.382-26T>C
NM_001172626.2:c.370-26T>C NP_001166097.2:n.370-26T>C