Canonical Allele Identifier: CA1190276249

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677294A= , CM000663.2:g.114677294A=	GRCh38
NC_000001.10:g.115219915A= , CM000663.1:g.115219915A=	GRCh37
NC_000001.9:g.115021438A=	NCBI36
NG_008012.1:g.23262T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1376+57T=	ENSP00000358551.4:n.1376+57T=
ENST00000520113.7:c.1388+57T= MANE Select	ENSP00000430075.3:n.1388+57T=
ENST00000637080.1:c.1171+57T=	ENSP00000489753.1:n.1171+57T=
ENST00000639077.1:n.1053+57T=
ENST00000369538.3:c.1475+57T=	ENSP00000358551.3:n.1475+57T=
ENST00000520113.6:c.1487+57T=	ENSP00000430075.2:n.1487+57T=
NM_000036.2:c.1487+57T=	NP_000027.2:n.1487+57T=
NM_001172626.1:c.1475+57T=	NP_001166097.1:n.1475+57T=
NM_000036.3:c.1388+57T= MANE Select	NP_000027.3:n.1388+57T=
NM_001172626.2:c.1376+57T=	NP_001166097.2:n.1376+57T=