Canonical Allele Identifier: CA341748976

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220547A>T (hg19) ; chr1:g.114677926A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677926A>T , CM000663.2:g.114677926A>T	GRCh38
NC_000001.10:g.115220547A>T , CM000663.1:g.115220547A>T	GRCh37
NC_000001.9:g.115022070A>T	NCBI36
NG_008012.1:g.22630T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.1196T>A	ENSP00000358551.4:p.Phe399Tyr
ENST00000520113.7:c.1208T>A MANE Select	ENSP00000430075.3:p.Phe403Tyr
ENST00000637080.1:c.991T>A	ENSP00000489753.1:n.991T>A
ENST00000639077.1:n.873T>A
ENST00000369538.3:c.1295T>A	ENSP00000358551.3:p.Phe432Tyr
ENST00000520113.6:c.1307T>A	ENSP00000430075.2:p.Phe436Tyr
NM_000036.2:c.1307T>A	NP_000027.2:p.Phe436Tyr
NM_001172626.1:c.1295T>A	NP_001166097.1:p.Phe432Tyr
NM_000036.3:c.1208T>A MANE Select	NP_000027.3:p.Phe403Tyr
NM_001172626.2:c.1196T>A	NP_001166097.2:p.Phe399Tyr