Canonical Allele Identifier: CA419883519

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226929T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684308T>G , CM000663.2:g.114684308T>G	GRCh38
NC_000001.10:g.115226929T>G , CM000663.1:g.115226929T>G	GRCh37
NC_000001.9:g.115028452T>G	NCBI36
NG_008012.1:g.16248A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.426A>C	ENSP00000358551.4:p.Ile142=
ENST00000520113.7:c.438A>C MANE Select	ENSP00000430075.3:p.Ile146=
ENST00000637080.1:c.441A>C	ENSP00000489753.1:p.Ile147=
ENST00000639077.1:n.103A>C
ENST00000369538.3:c.525A>C	ENSP00000358551.3:p.Ile175=
ENST00000485564.3:n.312A>C
ENST00000520113.6:c.537A>C	ENSP00000430075.2:p.Ile179=
NM_000036.2:c.537A>C	NP_000027.2:p.Ile179=
NM_001172626.1:c.525A>C	NP_001166097.1:p.Ile175=
NM_000036.3:c.438A>C MANE Select	NP_000027.3:p.Ile146=
NM_001172626.2:c.426A>C	NP_001166097.2:p.Ile142=