Canonical Allele Identifier: CA2269949979

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497162C= , CM000679.2:g.63497162C=	GRCh38
NC_000017.10:g.61574523C= , CM000679.1:g.61574523C=	GRCh37
NC_000017.9:g.58928255C=	NCBI36
NG_011648.1:g.25090C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3717C= MANE Select	ENSP00000290866.4:p.Asp1239=
ENST00000290863.10:c.1995C=	ENSP00000290863.6:p.Asp665=
ENST00000290866.9:c.3717C=	ENSP00000290866.4:p.Asp1239=
ENST00000413513.7:c.1872C=	ENSP00000392247.3:p.Asp624=
ENST00000428043.5:c.*139C=	ENSP00000397593.2:n.*139C=
ENST00000577418.5:n.727C=
ENST00000577647.2:c.1969+177C=	ENSP00000464149.1:n.1969+177C=
ENST00000578839.5:c.*1472C=	ENSP00000462110.2:n.*1472C=
ENST00000579314.5:c.*1446C=	ENSP00000462599.1:n.*1446C=
NM_000789.3:c.3717C=	NP_000780.1:p.Asp1239=
NM_001178057.1:c.1872C=	NP_001171528.1:p.Asp624=
NM_152830.2:c.1995C=	NP_690043.1:p.Asp665=
XM_005257110.1:c.3168C=	XP_005257167.1:p.Asp1056=
XM_006721737.2:c.2055C=	XP_006721800.2:p.Asp685=
XM_006721737.3:c.2055C=	XP_006721800.2:p.Asp685=
NM_000789.4:c.3717C= MANE Select	NP_000780.1:p.Asp1239=
NM_001178057.2:c.1872C=	NP_001171528.1:p.Asp624=
NM_152830.3:c.1995C=	NP_690043.1:p.Asp665=
NM_001382700.1:c.3150C=	NP_001369629.1:p.Asp1050=
NM_001382701.1:c.2865C=	NP_001369630.1:p.Asp955=
NM_001382702.1:c.1332C=	NP_001369631.1:p.Asp444=
NR_168483.1:n.2095C=