Canonical Allele Identifier: CA341752735

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226937G>T (hg19) ; chr1:g.114684316G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684316G>T , CM000663.2:g.114684316G>T	GRCh38
NC_000001.10:g.115226937G>T , CM000663.1:g.115226937G>T	GRCh37
NC_000001.9:g.115028460G>T	NCBI36
NG_008012.1:g.16240C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.418C>A	ENSP00000358551.4:p.Leu140Ile
ENST00000520113.7:c.430C>A MANE Select	ENSP00000430075.3:p.Leu144Ile
ENST00000637080.1:c.433C>A	ENSP00000489753.1:p.Leu145Ile
ENST00000639077.1:n.95C>A
ENST00000369538.3:c.517C>A	ENSP00000358551.3:p.Leu173Ile
ENST00000485564.3:n.304C>A
ENST00000520113.6:c.529C>A	ENSP00000430075.2:p.Leu177Ile
NM_000036.2:c.529C>A	NP_000027.2:p.Leu177Ile
NM_001172626.1:c.517C>A	NP_001166097.1:p.Leu173Ile
NM_000036.3:c.430C>A MANE Select	NP_000027.3:p.Leu144Ile
NM_001172626.2:c.418C>A	NP_001166097.2:p.Leu140Ile