Canonical Allele Identifier: CA2269945996

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488789A= , CM000679.2:g.63488789A=	GRCh38
NC_000017.10:g.61566150A= , CM000679.1:g.61566150A=	GRCh37
NC_000017.9:g.58919882A=	NCBI36
NG_011648.1:g.16717A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2447A= MANE Select	ENSP00000290866.4:p.Asn816=
ENST00000290863.10:c.725A=	ENSP00000290863.6:p.Asn242=
ENST00000290866.9:c.2447A=	ENSP00000290866.4:p.Asn816=
ENST00000413513.7:c.725A=	ENSP00000392247.3:p.Asn242=
ENST00000428043.5:c.2447A=	ENSP00000397593.2:p.Asn816=
ENST00000577647.2:c.725A=	ENSP00000464149.1:p.Asn242=
ENST00000578839.5:c.*517A=	ENSP00000462110.2:n.*517A=
ENST00000579204.1:c.706A=	ENSP00000464629.1:n.706A=
ENST00000579314.5:c.*176A=	ENSP00000462599.1:n.*176A=
ENST00000582005.5:c.*367A=	ENSP00000462002.1:n.*367A=
ENST00000582761.1:c.215A=	ENSP00000462909.1:p.Asn72=
ENST00000584865.5:n.393A=
NM_000789.3:c.2447A=	NP_000780.1:p.Asn816=
NM_001178057.1:c.725A=	NP_001171528.1:p.Asn242=
NM_152830.2:c.725A=	NP_690043.1:p.Asn242=
XM_005257110.1:c.1898A=	XP_005257167.1:p.Asn633=
XM_006721737.2:c.785A=	XP_006721800.2:p.Asn262=
XM_006721737.3:c.785A=	XP_006721800.2:p.Asn262=
NM_000789.4:c.2447A= MANE Select	NP_000780.1:p.Asn816=
NM_001178057.2:c.725A=	NP_001171528.1:p.Asn242=
NM_152830.3:c.725A=	NP_690043.1:p.Asn242=
NM_001382700.1:c.1880A=	NP_001369629.1:p.Asn627=
NM_001382701.1:c.1595A=	NP_001369630.1:p.Asn532=
NM_001382702.1:c.377A=	NP_001369631.1:p.Asn126=
NR_168483.1:n.825A=