Canonical Allele Identifier: CA1190282059

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684404C= , CM000663.2:g.114684404C=	GRCh38
NC_000001.10:g.115227025C= , CM000663.1:g.115227025C=	GRCh37
NC_000001.9:g.115028548C=	NCBI36
NG_008012.1:g.16152G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.370-40G=	ENSP00000358551.4:n.370-40G=
ENST00000520113.7:c.382-40G= MANE Select	ENSP00000430075.3:n.382-40G=
ENST00000637080.1:c.385-40G=	ENSP00000489753.1:n.385-40G=
ENST00000639077.1:n.47-40G=
ENST00000369538.3:c.469-40G=	ENSP00000358551.3:n.469-40G=
ENST00000485564.3:n.256-40G=
ENST00000520113.6:c.481-40G=	ENSP00000430075.2:n.481-40G=
NM_000036.2:c.481-40G=	NP_000027.2:n.481-40G=
NM_001172626.1:c.469-40G=	NP_001166097.1:n.469-40G=
NM_000036.3:c.382-40G= MANE Select	NP_000027.3:n.382-40G=
NM_001172626.2:c.370-40G=	NP_001166097.2:n.370-40G=