Canonical Allele Identifier: CA341749117
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677990C>T , CM000663.2:g.114677990C>T GRCh38
NC_000001.10:g.115220611C>T , CM000663.1:g.115220611C>T GRCh37
NC_000001.9:g.115022134C>T NCBI36
NG_008012.1:g.22566G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1132G>A ENSP00000358551.4:p.Val378Ile
ENST00000520113.7:c.1144G>A MANE Select ENSP00000430075.3:p.Val382Ile
ENST00000637080.1:c.927G>A ENSP00000489753.1:n.927G>A
ENST00000639077.1:n.809G>A
ENST00000369538.3:c.1231G>A ENSP00000358551.3:p.Val411Ile
ENST00000520113.6:c.1243G>A ENSP00000430075.2:p.Val415Ile
NM_000036.2:c.1243G>A NP_000027.2:p.Val415Ile
NM_001172626.1:c.1231G>A NP_001166097.1:p.Val411Ile
NM_000036.3:c.1144G>A MANE Select NP_000027.3:p.Val382Ile
NM_001172626.2:c.1132G>A NP_001166097.2:p.Val378Ile