Canonical Allele Identifier: CA419883286

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115222248T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114679627T>C , CM000663.2:g.114679627T>C	GRCh38
NC_000001.10:g.115222248T>C , CM000663.1:g.115222248T>C	GRCh37
NC_000001.9:g.115023771T>C	NCBI36
NG_008012.1:g.20929A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.837A>G	ENSP00000358551.4:p.Leu279=
ENST00000520113.7:c.849A>G MANE Select	ENSP00000430075.3:p.Leu283=
ENST00000637080.1:c.632A>G	ENSP00000489753.1:n.632A>G
ENST00000639077.1:n.514A>G
ENST00000369538.3:c.936A>G	ENSP00000358551.3:p.Leu312=
ENST00000520113.6:c.948A>G	ENSP00000430075.2:p.Leu316=
NM_000036.2:c.948A>G	NP_000027.2:p.Leu316=
NM_001172626.1:c.936A>G	NP_001166097.1:p.Leu312=
NM_000036.3:c.849A>G MANE Select	NP_000027.3:p.Leu283=
NM_001172626.2:c.837A>G	NP_001166097.2:p.Leu279=