Canonical Allele Identifier: CA2269950067

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497329C= , CM000679.2:g.63497329C=	GRCh38
NC_000017.10:g.61574690C= , CM000679.1:g.61574690C=	GRCh37
NC_000017.9:g.58928422C=	NCBI36
NG_011648.1:g.25257C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3884C= MANE Select	ENSP00000290866.4:p.Pro1295=
ENST00000290863.10:c.2162C=	ENSP00000290863.6:p.Pro721=
ENST00000290866.9:c.3884C=	ENSP00000290866.4:p.Pro1295=
ENST00000413513.7:c.2039C=	ENSP00000392247.3:p.Pro680=
ENST00000428043.5:c.*306C=	ENSP00000397593.2:n.*306C=
ENST00000577647.2:c.1969+344C=	ENSP00000464149.1:n.1969+344C=
ENST00000578839.5:c.*1639C=	ENSP00000462110.2:n.*1639C=
ENST00000579314.5:c.*1613C=	ENSP00000462599.1:n.*1613C=
NM_000789.3:c.3884C=	NP_000780.1:p.Pro1295=
NM_001178057.1:c.2039C=	NP_001171528.1:p.Pro680=
NM_152830.2:c.2162C=	NP_690043.1:p.Pro721=
XM_005257110.1:c.3335C=	XP_005257167.1:p.Pro1112=
XM_006721737.2:c.2222C=	XP_006721800.2:p.Pro741=
XM_006721737.3:c.2222C=	XP_006721800.2:p.Pro741=
NM_000789.4:c.3884C= MANE Select	NP_000780.1:p.Pro1295=
NM_001178057.2:c.2039C=	NP_001171528.1:p.Pro680=
NM_152830.3:c.2162C=	NP_690043.1:p.Pro721=
NM_001382700.1:c.3317C=	NP_001369629.1:p.Pro1106=
NM_001382701.1:c.3032C=	NP_001369630.1:p.Pro1011=
NM_001382702.1:c.1499C=	NP_001369631.1:p.Pro500=
NR_168483.1:n.2262C=