Canonical Allele Identifier: CA2269945937

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488669C= , CM000679.2:g.63488669C=	GRCh38
NC_000017.10:g.61566030C= , CM000679.1:g.61566030C=	GRCh37
NC_000017.9:g.58919762C=	NCBI36
NG_011648.1:g.16597C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2327C= MANE Select	ENSP00000290866.4:p.Thr776=
ENST00000290863.10:c.605C=	ENSP00000290863.6:p.Thr202=
ENST00000290866.9:c.2327C=	ENSP00000290866.4:p.Thr776=
ENST00000413513.7:c.605C=	ENSP00000392247.3:p.Thr202=
ENST00000428043.5:c.2327C=	ENSP00000397593.2:p.Thr776=
ENST00000577647.2:c.605C=	ENSP00000464149.1:p.Thr202=
ENST00000578839.5:c.*397C=	ENSP00000462110.2:n.*397C=
ENST00000579204.1:c.586C=	ENSP00000464629.1:n.586C=
ENST00000579314.5:c.*56C=	ENSP00000462599.1:n.*56C=
ENST00000582005.5:c.*247C=	ENSP00000462002.1:n.*247C=
ENST00000582761.1:c.95C=	ENSP00000462909.1:p.Thr32=
ENST00000584865.5:n.273C=
NM_000789.3:c.2327C=	NP_000780.1:p.Thr776=
NM_001178057.1:c.605C=	NP_001171528.1:p.Thr202=
NM_152830.2:c.605C=	NP_690043.1:p.Thr202=
XM_005257110.1:c.1778C=	XP_005257167.1:p.Thr593=
XM_006721737.2:c.665C=	XP_006721800.2:p.Thr222=
XM_006721737.3:c.665C=	XP_006721800.2:p.Thr222=
NM_000789.4:c.2327C= MANE Select	NP_000780.1:p.Thr776=
NM_001178057.2:c.605C=	NP_001171528.1:p.Thr202=
NM_152830.3:c.605C=	NP_690043.1:p.Thr202=
NM_001382700.1:c.1760C=	NP_001369629.1:p.Thr587=
NM_001382701.1:c.1475C=	NP_001369630.1:p.Thr492=
NM_001382702.1:c.257C=	NP_001369631.1:p.Thr86=
NR_168483.1:n.705C=