Canonical Allele Identifier: CA2647253913
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684459T>A , CM000663.2:g.114684459T>A GRCh38
NC_000001.10:g.115227080T>A , CM000663.1:g.115227080T>A GRCh37
NC_000001.9:g.115028603T>A NCBI36
NG_008012.1:g.16097A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.370-95A>T ENSP00000358551.4:n.370-95A>T
ENST00000520113.7:c.382-95A>T MANE Select ENSP00000430075.3:n.382-95A>T
ENST00000637080.1:c.385-95A>T ENSP00000489753.1:n.385-95A>T
ENST00000639077.1:n.31A>T
ENST00000369538.3:c.469-95A>T ENSP00000358551.3:n.469-95A>T
ENST00000485564.3:n.256-95A>T
ENST00000520113.6:c.481-95A>T ENSP00000430075.2:n.481-95A>T
NM_000036.2:c.481-95A>T NP_000027.2:n.481-95A>T
NM_001172626.1:c.469-95A>T NP_001166097.1:n.469-95A>T
NM_000036.3:c.382-95A>T MANE Select NP_000027.3:n.382-95A>T
NM_001172626.2:c.370-95A>T NP_001166097.2:n.370-95A>T