Canonical Allele Identifier: CA2269944861

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486644A= , CM000679.2:g.63486644A=	GRCh38
NC_000017.10:g.61564005A= , CM000679.1:g.61564005A=	GRCh37
NC_000017.9:g.58917737A=	NCBI36
NG_011648.1:g.14572A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2146A= MANE Select	ENSP00000290866.4:p.Thr716=
ENST00000290863.10:c.424A=	ENSP00000290863.6:p.Thr142=
ENST00000290866.9:c.2146A=	ENSP00000290866.4:p.Thr716=
ENST00000413513.7:c.424A=	ENSP00000392247.3:p.Thr142=
ENST00000428043.5:c.2146A=	ENSP00000397593.2:p.Thr716=
ENST00000577647.2:c.424A=	ENSP00000464149.1:p.Thr142=
ENST00000578839.5:c.*216A=	ENSP00000462110.2:n.*216A=
ENST00000579204.1:c.327A=	ENSP00000464629.1:n.327A=
ENST00000579314.5:c.424A=	ENSP00000462599.1:p.Thr142=
ENST00000579726.5:c.708A=
ENST00000582005.5:c.*66A=	ENSP00000462002.1:n.*66A=
NM_000789.3:c.2146A=	NP_000780.1:p.Thr716=
NM_001178057.1:c.424A=	NP_001171528.1:p.Thr142=
NM_152830.2:c.424A=	NP_690043.1:p.Thr142=
XM_005257110.1:c.1597A=	XP_005257167.1:p.Thr533=
XM_006721737.2:c.484A=	XP_006721800.2:p.Thr162=
XM_006721737.3:c.484A=	XP_006721800.2:p.Thr162=
NM_000789.4:c.2146A= MANE Select	NP_000780.1:p.Thr716=
NM_001178057.2:c.424A=	NP_001171528.1:p.Thr142=
NM_152830.3:c.424A=	NP_690043.1:p.Thr142=
NM_001382700.1:c.1579A=	NP_001369629.1:p.Thr527=
NM_001382701.1:c.1294A=	NP_001369630.1:p.Thr432=
NM_001382702.1:c.76A=	NP_001369631.1:p.Thr26=
NR_168483.1:n.446A=