Canonical Allele Identifier: CA341752688

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226923C>G (hg19) ; chr1:g.114684302C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684302C>G , CM000663.2:g.114684302C>G	GRCh38
NC_000001.10:g.115226923C>G , CM000663.1:g.115226923C>G	GRCh37
NC_000001.9:g.115028446C>G	NCBI36
NG_008012.1:g.16254G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.432G>C	ENSP00000358551.4:p.Glu144Asp
ENST00000520113.7:c.444G>C MANE Select	ENSP00000430075.3:p.Glu148Asp
ENST00000637080.1:c.447G>C	ENSP00000489753.1:p.Glu149Asp
ENST00000639077.1:n.109G>C
ENST00000369538.3:c.531G>C	ENSP00000358551.3:p.Glu177Asp
ENST00000485564.3:n.318G>C
ENST00000520113.6:c.543G>C	ENSP00000430075.2:p.Glu181Asp
NM_000036.2:c.543G>C	NP_000027.2:p.Glu181Asp
NM_001172626.1:c.531G>C	NP_001166097.1:p.Glu177Asp
NM_000036.3:c.444G>C MANE Select	NP_000027.3:p.Glu148Asp
NM_001172626.2:c.432G>C	NP_001166097.2:p.Glu144Asp