Canonical Allele Identifier: CA2269946134

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63489052C= , CM000679.2:g.63489052C=	GRCh38
NC_000017.10:g.61566413C= , CM000679.1:g.61566413C=	GRCh37
NC_000017.9:g.58920145C=	NCBI36
NG_011648.1:g.16980C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2561C= MANE Select	ENSP00000290866.4:p.Ala854=
ENST00000290863.10:c.839C=	ENSP00000290863.6:p.Ala280=
ENST00000290866.9:c.2561C=	ENSP00000290866.4:p.Ala854=
ENST00000413513.7:c.839C=	ENSP00000392247.3:p.Ala280=
ENST00000428043.5:c.2561C=	ENSP00000397593.2:p.Ala854=
ENST00000577647.2:c.839C=	ENSP00000464149.1:p.Ala280=
ENST00000578839.5:c.*519+261C=	ENSP00000462110.2:n.*519+261C=
ENST00000579314.5:c.*290C=	ENSP00000462599.1:n.*290C=
ENST00000582005.5:c.*481C=	ENSP00000462002.1:n.*481C=
ENST00000582761.1:c.329C=	ENSP00000462909.1:p.Ala110=
ENST00000584865.5:n.507C=
NM_000789.3:c.2561C=	NP_000780.1:p.Ala854=
NM_001178057.1:c.839C=	NP_001171528.1:p.Ala280=
NM_152830.2:c.839C=	NP_690043.1:p.Ala280=
XM_005257110.1:c.2012C=	XP_005257167.1:p.Ala671=
XM_006721737.2:c.899C=	XP_006721800.2:p.Ala300=
XM_006721737.3:c.899C=	XP_006721800.2:p.Ala300=
NM_000789.4:c.2561C= MANE Select	NP_000780.1:p.Ala854=
NM_001178057.2:c.839C=	NP_001171528.1:p.Ala280=
NM_152830.3:c.839C=	NP_690043.1:p.Ala280=
NM_001382700.1:c.1994C=	NP_001369629.1:p.Ala665=
NM_001382701.1:c.1709C=	NP_001369630.1:p.Ala570=
NM_001382702.1:c.379+261C=	NP_001369631.1:n.379+261C=
NR_168483.1:n.939C=