Canonical Allele Identifier: CA2269945932

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488658T= , CM000679.2:g.63488658T=	GRCh38
NC_000017.10:g.61566019T= , CM000679.1:g.61566019T=	GRCh37
NC_000017.9:g.58919751T=	NCBI36
NG_011648.1:g.16586T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2316T= MANE Select	ENSP00000290866.4:p.Asn772=
ENST00000290863.10:c.594T=	ENSP00000290863.6:p.Asn198=
ENST00000290866.9:c.2316T=	ENSP00000290866.4:p.Asn772=
ENST00000413513.7:c.594T=	ENSP00000392247.3:p.Asn198=
ENST00000428043.5:c.2316T=	ENSP00000397593.2:p.Asn772=
ENST00000577647.2:c.594T=	ENSP00000464149.1:p.Asn198=
ENST00000578839.5:c.*386T=	ENSP00000462110.2:n.*386T=
ENST00000579204.1:c.575T=	ENSP00000464629.1:n.575T=
ENST00000579314.5:c.*45T=	ENSP00000462599.1:n.*45T=
ENST00000582005.5:c.*236T=	ENSP00000462002.1:n.*236T=
ENST00000582761.1:c.84T=	ENSP00000462909.1:p.Asn28=
ENST00000584865.5:n.262T=
NM_000789.3:c.2316T=	NP_000780.1:p.Asn772=
NM_001178057.1:c.594T=	NP_001171528.1:p.Asn198=
NM_152830.2:c.594T=	NP_690043.1:p.Asn198=
XM_005257110.1:c.1767T=	XP_005257167.1:p.Asn589=
XM_006721737.2:c.654T=	XP_006721800.2:p.Asn218=
XM_006721737.3:c.654T=	XP_006721800.2:p.Asn218=
NM_000789.4:c.2316T= MANE Select	NP_000780.1:p.Asn772=
NM_001178057.2:c.594T=	NP_001171528.1:p.Asn198=
NM_152830.3:c.594T=	NP_690043.1:p.Asn198=
NM_001382700.1:c.1749T=	NP_001369629.1:p.Asn583=
NM_001382701.1:c.1464T=	NP_001369630.1:p.Asn488=
NM_001382702.1:c.246T=	NP_001369631.1:p.Asn82=
NR_168483.1:n.694T=