Canonical Allele Identifier: CA419883288

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115222251C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114679630C>T , CM000663.2:g.114679630C>T	GRCh38
NC_000001.10:g.115222251C>T , CM000663.1:g.115222251C>T	GRCh37
NC_000001.9:g.115023774C>T	NCBI36
NG_008012.1:g.20926G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.834G>A	ENSP00000358551.4:p.Glu278=
ENST00000520113.7:c.846G>A MANE Select	ENSP00000430075.3:p.Glu282=
ENST00000637080.1:c.629G>A	ENSP00000489753.1:n.629G>A
ENST00000639077.1:n.511G>A
ENST00000369538.3:c.933G>A	ENSP00000358551.3:p.Glu311=
ENST00000520113.6:c.945G>A	ENSP00000430075.2:p.Glu315=
NM_000036.2:c.945G>A	NP_000027.2:p.Glu315=
NM_001172626.1:c.933G>A	NP_001166097.1:p.Glu311=
NM_000036.3:c.846G>A MANE Select	NP_000027.3:p.Glu282=
NM_001172626.2:c.834G>A	NP_001166097.2:p.Glu278=