Canonical Allele Identifier: CA1190281968

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684361T= , CM000663.2:g.114684361T=	GRCh38
NC_000001.10:g.115226982T= , CM000663.1:g.115226982T=	GRCh37
NC_000001.9:g.115028505T=	NCBI36
NG_008012.1:g.16195A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.373A=	ENSP00000358551.4:p.Thr125=
ENST00000520113.7:c.385A= MANE Select	ENSP00000430075.3:p.Thr129=
ENST00000637080.1:c.388A=	ENSP00000489753.1:p.Thr130=
ENST00000639077.1:n.50A=
ENST00000369538.3:c.472A=	ENSP00000358551.3:p.Thr158=
ENST00000485564.3:n.259A=
ENST00000520113.6:c.484A=	ENSP00000430075.2:p.Thr162=
NM_000036.2:c.484A=	NP_000027.2:p.Thr162=
NM_001172626.1:c.472A=	NP_001166097.1:p.Thr158=
NM_000036.3:c.385A= MANE Select	NP_000027.3:p.Thr129=
NM_001172626.2:c.373A=	NP_001166097.2:p.Thr125=