Canonical Allele Identifier: CA2269942597

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482466G= , CM000679.2:g.63482466G=	GRCh38
NC_000017.10:g.61559827G= , CM000679.1:g.61559827G=	GRCh37
NC_000017.9:g.58913559G=	NCBI36
NG_011648.1:g.10394G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1119G= MANE Select	ENSP00000290866.4:p.Arg373=
ENST00000290866.9:c.1119G=	ENSP00000290866.4:p.Arg373=
ENST00000428043.5:c.1119G=	ENSP00000397593.2:p.Arg373=
ENST00000582678.5:c.*518G=	ENSP00000462995.1:n.*518G=
ENST00000584529.5:n.1153G=
NM_000789.3:c.1119G=	NP_000780.1:p.Arg373=
XM_005257110.1:c.570G=	XP_005257167.1:p.Arg190=
NM_000789.4:c.1119G= MANE Select	NP_000780.1:p.Arg373=
NM_001382700.1:c.552G=	NP_001369629.1:p.Arg184=
NM_001382701.1:c.267G=	NP_001369630.1:p.Arg89=