Canonical Allele Identifier: CA1190276599

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677928A= , CM000663.2:g.114677928A=	GRCh38
NC_000001.10:g.115220549A= , CM000663.1:g.115220549A=	GRCh37
NC_000001.9:g.115022072A=	NCBI36
NG_008012.1:g.22628T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.1194T=	ENSP00000358551.4:p.Tyr398=
ENST00000520113.7:c.1206T= MANE Select	ENSP00000430075.3:p.Tyr402=
ENST00000637080.1:c.989T=	ENSP00000489753.1:n.989T=
ENST00000639077.1:n.871T=
ENST00000369538.3:c.1293T=	ENSP00000358551.3:p.Tyr431=
ENST00000520113.6:c.1305T=	ENSP00000430075.2:p.Tyr435=
NM_000036.2:c.1305T=	NP_000027.2:p.Tyr435=
NM_001172626.1:c.1293T=	NP_001166097.1:p.Tyr431=
NM_000036.3:c.1206T= MANE Select	NP_000027.3:p.Tyr402=
NM_001172626.2:c.1194T=	NP_001166097.2:p.Tyr398=