Canonical Allele Identifier: CA341752322

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226836A>T (hg19) ; chr1:g.114684215A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684215A>T , CM000663.2:g.114684215A>T	GRCh38
NC_000001.10:g.115226836A>T , CM000663.1:g.115226836A>T	GRCh37
NC_000001.9:g.115028359A>T	NCBI36
NG_008012.1:g.16341T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.519T>A	ENSP00000358551.4:p.Asn173Lys
ENST00000520113.7:c.531T>A MANE Select	ENSP00000430075.3:p.Asn177Lys
ENST00000637080.1:c.534T>A	ENSP00000489753.1:p.Asn178Lys
ENST00000639077.1:n.196T>A
ENST00000369538.3:c.618T>A	ENSP00000358551.3:p.Asn206Lys
ENST00000485564.3:n.405T>A
ENST00000520113.6:c.630T>A	ENSP00000430075.2:p.Asn210Lys
NM_000036.2:c.630T>A	NP_000027.2:p.Asn210Lys
NM_001172626.1:c.618T>A	NP_001166097.1:p.Asn206Lys
NM_000036.3:c.531T>A MANE Select	NP_000027.3:p.Asn177Lys
NM_001172626.2:c.519T>A	NP_001166097.2:p.Asn173Lys