Canonical Allele Identifier: CA1190282032

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684384C= , CM000663.2:g.114684384C=	GRCh38
NC_000001.10:g.115227005C= , CM000663.1:g.115227005C=	GRCh37
NC_000001.9:g.115028528C=	NCBI36
NG_008012.1:g.16172G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.370-20G=	ENSP00000358551.4:n.370-20G=
ENST00000520113.7:c.382-20G= MANE Select	ENSP00000430075.3:n.382-20G=
ENST00000637080.1:c.385-20G=	ENSP00000489753.1:n.385-20G=
ENST00000639077.1:n.47-20G=
ENST00000369538.3:c.469-20G=	ENSP00000358551.3:n.469-20G=
ENST00000485564.3:n.256-20G=
ENST00000520113.6:c.481-20G=	ENSP00000430075.2:n.481-20G=
NM_000036.2:c.481-20G=	NP_000027.2:n.481-20G=
NM_001172626.1:c.469-20G=	NP_001166097.1:n.469-20G=
NM_000036.3:c.382-20G= MANE Select	NP_000027.3:n.382-20G=
NM_001172626.2:c.370-20G=	NP_001166097.2:n.370-20G=