Canonical Allele Identifier: CA1190281767

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684233A= , CM000663.2:g.114684233A=	GRCh38
NC_000001.10:g.115226854A= , CM000663.1:g.115226854A=	GRCh37
NC_000001.9:g.115028377A=	NCBI36
NG_008012.1:g.16323T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.501T=	ENSP00000358551.4:p.Gly167=
ENST00000520113.7:c.513T= MANE Select	ENSP00000430075.3:p.Gly171=
ENST00000637080.1:c.516T=	ENSP00000489753.1:p.Gly172=
ENST00000639077.1:n.178T=
ENST00000369538.3:c.600T=	ENSP00000358551.3:p.Gly200=
ENST00000485564.3:n.387T=
ENST00000520113.6:c.612T=	ENSP00000430075.2:p.Gly204=
NM_000036.2:c.612T=	NP_000027.2:p.Gly204=
NM_001172626.1:c.600T=	NP_001166097.1:p.Gly200=
NM_000036.3:c.513T= MANE Select	NP_000027.3:p.Gly171=
NM_001172626.2:c.501T=	NP_001166097.2:p.Gly167=