Canonical Allele Identifier: CA2269945990

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488777C= , CM000679.2:g.63488777C=	GRCh38
NC_000017.10:g.61566138C= , CM000679.1:g.61566138C=	GRCh37
NC_000017.9:g.58919870C=	NCBI36
NG_011648.1:g.16705C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2435C= MANE Select	ENSP00000290866.4:p.Ala812=
ENST00000290863.10:c.713C=	ENSP00000290863.6:p.Ala238=
ENST00000290866.9:c.2435C=	ENSP00000290866.4:p.Ala812=
ENST00000413513.7:c.713C=	ENSP00000392247.3:p.Ala238=
ENST00000428043.5:c.2435C=	ENSP00000397593.2:p.Ala812=
ENST00000577647.2:c.713C=	ENSP00000464149.1:p.Ala238=
ENST00000578839.5:c.*505C=	ENSP00000462110.2:n.*505C=
ENST00000579204.1:c.694C=	ENSP00000464629.1:n.694C=
ENST00000579314.5:c.*164C=	ENSP00000462599.1:n.*164C=
ENST00000582005.5:c.*355C=	ENSP00000462002.1:n.*355C=
ENST00000582761.1:c.203C=	ENSP00000462909.1:p.Ala68=
ENST00000584865.5:n.381C=
NM_000789.3:c.2435C=	NP_000780.1:p.Ala812=
NM_001178057.1:c.713C=	NP_001171528.1:p.Ala238=
NM_152830.2:c.713C=	NP_690043.1:p.Ala238=
XM_005257110.1:c.1886C=	XP_005257167.1:p.Ala629=
XM_006721737.2:c.773C=	XP_006721800.2:p.Ala258=
XM_006721737.3:c.773C=	XP_006721800.2:p.Ala258=
NM_000789.4:c.2435C= MANE Select	NP_000780.1:p.Ala812=
NM_001178057.2:c.713C=	NP_001171528.1:p.Ala238=
NM_152830.3:c.713C=	NP_690043.1:p.Ala238=
NM_001382700.1:c.1868C=	NP_001369629.1:p.Ala623=
NM_001382701.1:c.1583C=	NP_001369630.1:p.Ala528=
NM_001382702.1:c.365C=	NP_001369631.1:p.Ala122=
NR_168483.1:n.813C=