Canonical Allele Identifier: CA1190282142

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684482T= , CM000663.2:g.114684482T=	GRCh38
NC_000001.10:g.115227103T= , CM000663.1:g.115227103T=	GRCh37
NC_000001.9:g.115028626T=	NCBI36
NG_008012.1:g.16074A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.370-118A=	ENSP00000358551.4:n.370-118A=
ENST00000520113.7:c.382-118A= MANE Select	ENSP00000430075.3:n.382-118A=
ENST00000637080.1:c.385-118A=	ENSP00000489753.1:n.385-118A=
ENST00000639077.1:n.8A=
ENST00000369538.3:c.469-118A=	ENSP00000358551.3:n.469-118A=
ENST00000485564.3:n.256-118A=
ENST00000520113.6:c.481-118A=	ENSP00000430075.2:n.481-118A=
NM_000036.2:c.481-118A=	NP_000027.2:n.481-118A=
NM_001172626.1:c.469-118A=	NP_001166097.1:n.469-118A=
NM_000036.3:c.382-118A= MANE Select	NP_000027.3:n.382-118A=
NM_001172626.2:c.370-118A=	NP_001166097.2:n.370-118A=