Canonical Allele Identifier: CA1190276519

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677822C= , CM000663.2:g.114677822C=	GRCh38
NC_000001.10:g.115220443C= , CM000663.1:g.115220443C=	GRCh37
NC_000001.9:g.115021966C=	NCBI36
NG_008012.1:g.22734G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1212+88G=	ENSP00000358551.4:n.1212+88G=
ENST00000520113.7:c.1224+88G= MANE Select	ENSP00000430075.3:n.1224+88G=
ENST00000637080.1:c.1007+88G=	ENSP00000489753.1:n.1007+88G=
ENST00000639077.1:n.889+88G=
ENST00000369538.3:c.1311+88G=	ENSP00000358551.3:n.1311+88G=
ENST00000520113.6:c.1323+88G=	ENSP00000430075.2:n.1323+88G=
NM_000036.2:c.1323+88G=	NP_000027.2:n.1323+88G=
NM_001172626.1:c.1311+88G=	NP_001166097.1:n.1311+88G=
NM_000036.3:c.1224+88G= MANE Select	NP_000027.3:n.1224+88G=
NM_001172626.2:c.1212+88G=	NP_001166097.2:n.1212+88G=