Canonical Allele Identifier: CA341750085

Gene: AMPD1

Linked Data

• dbSNP Id: rs1658095581
• MyVariant Identifiers: chr1:g.115222252T>A (hg19) ; chr1:g.114679631T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114679631T>A , CM000663.2:g.114679631T>A	GRCh38
NC_000001.10:g.115222252T>A , CM000663.1:g.115222252T>A	GRCh37
NC_000001.9:g.115023775T>A	NCBI36
NG_008012.1:g.20925A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.833A>T	ENSP00000358551.4:p.Glu278Val
ENST00000520113.7:c.845A>T MANE Select	ENSP00000430075.3:p.Glu282Val
ENST00000637080.1:c.628A>T	ENSP00000489753.1:n.628A>T
ENST00000639077.1:n.510A>T
ENST00000369538.3:c.932A>T	ENSP00000358551.3:p.Glu311Val
ENST00000520113.6:c.944A>T	ENSP00000430075.2:p.Glu315Val
NM_000036.2:c.944A>T	NP_000027.2:p.Glu315Val
NM_001172626.1:c.932A>T	NP_001166097.1:p.Glu311Val
NM_000036.3:c.845A>T MANE Select	NP_000027.3:p.Glu282Val
NM_001172626.2:c.833A>T	NP_001166097.2:p.Glu278Val