Canonical Allele Identifier: CA2269950640

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498251C= , CM000679.2:g.63498251C=	GRCh38
NC_000017.10:g.61575612C= , CM000679.1:g.61575612C=	GRCh37
NC_000017.9:g.58929344C=	NCBI36
NG_011648.1:g.26179C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*885C= MANE Select	ENSP00000290866.4:n.*885C=
ENST00000290866.9:c.*885C=	ENSP00000290866.4:n.*885C=
ENST00000428043.5:c.*1228C=	ENSP00000397593.2:n.*1228C=
ENST00000577647.2:c.1969+1266C=	ENSP00000464149.1:n.1969+1266C=
NM_000789.3:c.*885C=	NP_000780.1:n.*885C=
NM_001178057.1:c.*885C=	NP_001171528.1:n.*885C=
NM_152830.2:c.*885C=	NP_690043.1:n.*885C=
XM_005257110.1:c.*885C=	XP_005257167.1:n.*885C=
XM_006721737.2:c.*885C=	XP_006721800.2:n.*885C=
NM_000789.4:c.*885C= MANE Select	NP_000780.1:n.*885C=
NM_001178057.2:c.*885C=	NP_001171528.1:n.*885C=
NM_152830.3:c.*885C=	NP_690043.1:n.*885C=
NM_001382700.1:c.*885C=	NP_001369629.1:n.*885C=
NM_001382701.1:c.*885C=	NP_001369630.1:n.*885C=
NM_001382702.1:c.*885C=	NP_001369631.1:n.*885C=
NR_168483.1:n.3184C=