Canonical Allele Identifier: CA1190281819

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684251G= , CM000663.2:g.114684251G=	GRCh38
NC_000001.10:g.115226872G= , CM000663.1:g.115226872G=	GRCh37
NC_000001.9:g.115028395G=	NCBI36
NG_008012.1:g.16305C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.483C=	ENSP00000358551.4:p.Tyr161=
ENST00000520113.7:c.495C= MANE Select	ENSP00000430075.3:p.Tyr165=
ENST00000637080.1:c.498C=	ENSP00000489753.1:p.Tyr166=
ENST00000639077.1:n.160C=
ENST00000369538.3:c.582C=	ENSP00000358551.3:p.Tyr194=
ENST00000485564.3:n.369C=
ENST00000520113.6:c.594C=	ENSP00000430075.2:p.Tyr198=
NM_000036.2:c.594C=	NP_000027.2:p.Tyr198=
NM_001172626.1:c.582C=	NP_001166097.1:p.Tyr194=
NM_000036.3:c.495C= MANE Select	NP_000027.3:p.Tyr165=
NM_001172626.2:c.483C=	NP_001166097.2:p.Tyr161=