Canonical Allele Identifier: CA341752816

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226963A>G (hg19) ; chr1:g.114684342A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684342A>G , CM000663.2:g.114684342A>G	GRCh38
NC_000001.10:g.115226963A>G , CM000663.1:g.115226963A>G	GRCh37
NC_000001.9:g.115028486A>G	NCBI36
NG_008012.1:g.16214T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.392T>C	ENSP00000358551.4:p.Ile131Thr
ENST00000520113.7:c.404T>C MANE Select	ENSP00000430075.3:p.Ile135Thr
ENST00000637080.1:c.407T>C	ENSP00000489753.1:p.Ile136Thr
ENST00000639077.1:n.69T>C
ENST00000369538.3:c.491T>C	ENSP00000358551.3:p.Ile164Thr
ENST00000485564.3:n.278T>C
ENST00000520113.6:c.503T>C	ENSP00000430075.2:p.Ile168Thr
NM_000036.2:c.503T>C	NP_000027.2:p.Ile168Thr
NM_001172626.1:c.491T>C	NP_001166097.1:p.Ile164Thr
NM_000036.3:c.404T>C MANE Select	NP_000027.3:p.Ile135Thr
NM_001172626.2:c.392T>C	NP_001166097.2:p.Ile131Thr