Canonical Allele Identifier: CA1190277222

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114679465C= , CM000663.2:g.114679465C=	GRCh38
NC_000001.10:g.115222086C= , CM000663.1:g.115222086C=	GRCh37
NC_000001.9:g.115023609C=	NCBI36
NG_008012.1:g.21091G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.885+114G=	ENSP00000358551.4:n.885+114G=
ENST00000520113.7:c.897+114G= MANE Select	ENSP00000430075.3:n.897+114G=
ENST00000637080.1:c.680+114G=	ENSP00000489753.1:n.680+114G=
ENST00000639077.1:n.562+114G=
ENST00000369538.3:c.984+114G=	ENSP00000358551.3:n.984+114G=
ENST00000520113.6:c.996+114G=	ENSP00000430075.2:n.996+114G=
NM_000036.2:c.996+114G=	NP_000027.2:n.996+114G=
NM_001172626.1:c.984+114G=	NP_001166097.1:n.984+114G=
NM_000036.3:c.897+114G= MANE Select	NP_000027.3:n.897+114G=
NM_001172626.2:c.885+114G=	NP_001166097.2:n.885+114G=