Canonical Allele Identifier: CA2269945079

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487031A= , CM000679.2:g.63487031A=	GRCh38
NC_000017.10:g.61564392A= , CM000679.1:g.61564392A=	GRCh37
NC_000017.9:g.58918124A=	NCBI36
NG_011648.1:g.14959A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2263A= MANE Select	ENSP00000290866.4:p.Thr755=
ENST00000290863.10:c.541A=	ENSP00000290863.6:p.Thr181=
ENST00000290866.9:c.2263A=	ENSP00000290866.4:p.Thr755=
ENST00000413513.7:c.541A=	ENSP00000392247.3:p.Thr181=
ENST00000428043.5:c.2263A=	ENSP00000397593.2:p.Thr755=
ENST00000577647.2:c.541A=	ENSP00000464149.1:p.Thr181=
ENST00000578839.5:c.*333A=	ENSP00000462110.2:n.*333A=
ENST00000579204.1:c.444A=	ENSP00000464629.1:n.444A=
ENST00000579314.5:c.541A=	ENSP00000462599.1:p.Thr181=
ENST00000579726.5:c.825A=
ENST00000582005.5:c.*183A=	ENSP00000462002.1:n.*183A=
ENST00000582761.1:c.31A=	ENSP00000462909.1:p.Thr11=
ENST00000584865.5:n.209A=
NM_000789.3:c.2263A=	NP_000780.1:p.Thr755=
NM_001178057.1:c.541A=	NP_001171528.1:p.Thr181=
NM_152830.2:c.541A=	NP_690043.1:p.Thr181=
XM_005257110.1:c.1714A=	XP_005257167.1:p.Thr572=
XM_006721737.2:c.601A=	XP_006721800.2:p.Thr201=
XM_006721737.3:c.601A=	XP_006721800.2:p.Thr201=
NM_000789.4:c.2263A= MANE Select	NP_000780.1:p.Thr755=
NM_001178057.2:c.541A=	NP_001171528.1:p.Thr181=
NM_152830.3:c.541A=	NP_690043.1:p.Thr181=
NM_001382700.1:c.1696A=	NP_001369629.1:p.Thr566=
NM_001382701.1:c.1411A=	NP_001369630.1:p.Thr471=
NM_001382702.1:c.193A=	NP_001369631.1:p.Thr65=
NR_168483.1:n.563A=