Canonical Allele Identifier: CA2269949802

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496915G= , CM000679.2:g.63496915G=	GRCh38
NC_000017.10:g.61574276G= , CM000679.1:g.61574276G=	GRCh37
NC_000017.9:g.58928008G=	NCBI36
NG_011648.1:g.24843G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3621G= MANE Select	ENSP00000290866.4:p.Trp1207=
ENST00000290863.10:c.1899G=	ENSP00000290863.6:p.Trp633=
ENST00000290866.9:c.3621G=	ENSP00000290866.4:p.Trp1207=
ENST00000413513.7:c.1776G=	ENSP00000392247.3:p.Trp592=
ENST00000428043.5:c.3621G=	ENSP00000397593.2:p.Trp1207=
ENST00000577418.5:n.631G=
ENST00000577647.2:c.1899G=	ENSP00000464149.1:p.Trp633=
ENST00000578839.5:c.*1376G=	ENSP00000462110.2:n.*1376G=
ENST00000579314.5:c.*1350G=	ENSP00000462599.1:n.*1350G=
ENST00000579409.1:c.308G=
ENST00000582244.1:n.495G=
NM_000789.3:c.3621G=	NP_000780.1:p.Trp1207=
NM_001178057.1:c.1776G=	NP_001171528.1:p.Trp592=
NM_152830.2:c.1899G=	NP_690043.1:p.Trp633=
XM_005257110.1:c.3072G=	XP_005257167.1:p.Trp1024=
XM_006721737.2:c.1959G=	XP_006721800.2:p.Trp653=
XM_006721737.3:c.1959G=	XP_006721800.2:p.Trp653=
NM_000789.4:c.3621G= MANE Select	NP_000780.1:p.Trp1207=
NM_001178057.2:c.1776G=	NP_001171528.1:p.Trp592=
NM_152830.3:c.1899G=	NP_690043.1:p.Trp633=
NM_001382700.1:c.3054G=	NP_001369629.1:p.Trp1018=
NM_001382701.1:c.2769G=	NP_001369630.1:p.Trp923=
NM_001382702.1:c.1236G=	NP_001369631.1:p.Trp412=
NR_168483.1:n.1999G=