Canonical Allele Identifier: CA2269941608

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63480699C= , CM000679.2:g.63480699C=	GRCh38
NC_000017.10:g.61558060C= , CM000679.1:g.61558060C=	GRCh37
NC_000017.9:g.58911792C=	NCBI36
NG_011648.1:g.8627C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.847+171C= MANE Select	ENSP00000290866.4:n.847+171C=
ENST00000290866.9:c.847+171C=	ENSP00000290866.4:n.847+171C=
ENST00000428043.5:c.847+171C=	ENSP00000397593.2:n.847+171C=
ENST00000582627.1:c.847+171C=	ENSP00000462280.1:n.847+171C=
ENST00000582678.5:c.*246+171C=	ENSP00000462995.1:n.*246+171C=
ENST00000584529.5:n.881+171C=
NM_000789.3:c.847+171C=	NP_000780.1:n.847+171C=
XM_005257110.1:c.298+171C=	XP_005257167.1:n.298+171C=
NM_000789.4:c.847+171C= MANE Select	NP_000780.1:n.847+171C=
NM_001382700.1:c.374+171C=	NP_001369629.1:n.374+171C=
NM_001382701.1:c.-6+171C=	NP_001369630.1:n.-6+171C=