Canonical Allele Identifier: CA419883549

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226977A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684356A>T , CM000663.2:g.114684356A>T	GRCh38
NC_000001.10:g.115226977A>T , CM000663.1:g.115226977A>T	GRCh37
NC_000001.9:g.115028500A>T	NCBI36
NG_008012.1:g.16200T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.378T>A	ENSP00000358551.4:p.Val126=
ENST00000520113.7:c.390T>A MANE Select	ENSP00000430075.3:p.Val130=
ENST00000637080.1:c.393T>A	ENSP00000489753.1:p.Val131=
ENST00000639077.1:n.55T>A
ENST00000369538.3:c.477T>A	ENSP00000358551.3:p.Val159=
ENST00000485564.3:n.264T>A
ENST00000520113.6:c.489T>A	ENSP00000430075.2:p.Val163=
NM_000036.2:c.489T>A	NP_000027.2:p.Val163=
NM_001172626.1:c.477T>A	NP_001166097.1:p.Val159=
NM_000036.3:c.390T>A MANE Select	NP_000027.3:p.Val130=
NM_001172626.2:c.378T>A	NP_001166097.2:p.Val126=