Canonical Allele Identifier: CA341752857

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226973C>A (hg19) ; chr1:g.114684352C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684352C>A , CM000663.2:g.114684352C>A	GRCh38
NC_000001.10:g.115226973C>A , CM000663.1:g.115226973C>A	GRCh37
NC_000001.9:g.115028496C>A	NCBI36
NG_008012.1:g.16204G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.382G>T	ENSP00000358551.4:p.Asp128Tyr
ENST00000520113.7:c.394G>T MANE Select	ENSP00000430075.3:p.Asp132Tyr
ENST00000637080.1:c.397G>T	ENSP00000489753.1:p.Asp133Tyr
ENST00000639077.1:n.59G>T
ENST00000369538.3:c.481G>T	ENSP00000358551.3:p.Asp161Tyr
ENST00000485564.3:n.268G>T
ENST00000520113.6:c.493G>T	ENSP00000430075.2:p.Asp165Tyr
NM_000036.2:c.493G>T	NP_000027.2:p.Asp165Tyr
NM_001172626.1:c.481G>T	NP_001166097.1:p.Asp161Tyr
NM_000036.3:c.394G>T MANE Select	NP_000027.3:p.Asp132Tyr
NM_001172626.2:c.382G>T	NP_001166097.2:p.Asp128Tyr