Canonical Allele Identifier: CA1141689258

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684278C= , CM000663.2:g.114684278C=	GRCh38
NC_000001.10:g.115226899C= , CM000663.1:g.115226899C=	GRCh37
NC_000001.9:g.115028422C=	NCBI36
NG_008012.1:g.16278G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.456G=	ENSP00000358551.4:p.Gln152=
ENST00000520113.7:c.468G= MANE Select	ENSP00000430075.3:p.Gln156=
ENST00000637080.1:c.471G=	ENSP00000489753.1:p.Gln157=
ENST00000639077.1:n.133G=
ENST00000369538.3:c.555G=	ENSP00000358551.3:p.Gln185=
ENST00000485564.3:n.342G=
ENST00000520113.6:c.567G=	ENSP00000430075.2:p.Gln189=
NM_000036.2:c.567G=	NP_000027.2:p.Gln189=
NM_001172626.1:c.555G=	NP_001166097.1:p.Gln185=
NM_000036.3:c.468G= MANE Select	NP_000027.3:p.Gln156=
NM_001172626.2:c.456G=	NP_001166097.2:p.Gln152=