Canonical Allele Identifier: CA341752629

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226909T>C (hg19) ; chr1:g.114684288T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684288T>C , CM000663.2:g.114684288T>C	GRCh38
NC_000001.10:g.115226909T>C , CM000663.1:g.115226909T>C	GRCh37
NC_000001.9:g.115028432T>C	NCBI36
NG_008012.1:g.16268A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.446A>G	ENSP00000358551.4:p.Lys149Arg
ENST00000520113.7:c.458A>G MANE Select	ENSP00000430075.3:p.Lys153Arg
ENST00000637080.1:c.461A>G	ENSP00000489753.1:p.Lys154Arg
ENST00000639077.1:n.123A>G
ENST00000369538.3:c.545A>G	ENSP00000358551.3:p.Lys182Arg
ENST00000485564.3:n.332A>G
ENST00000520113.6:c.557A>G	ENSP00000430075.2:p.Lys186Arg
NM_000036.2:c.557A>G	NP_000027.2:p.Lys186Arg
NM_001172626.1:c.545A>G	NP_001166097.1:p.Lys182Arg
NM_000036.3:c.458A>G MANE Select	NP_000027.3:p.Lys153Arg
NM_001172626.2:c.446A>G	NP_001166097.2:p.Lys149Arg