Canonical Allele Identifier: CA2269950509

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498055T= , CM000679.2:g.63498055T=	GRCh38
NC_000017.10:g.61575416T= , CM000679.1:g.61575416T=	GRCh37
NC_000017.9:g.58929148T=	NCBI36
NG_011648.1:g.25983T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*689T= MANE Select	ENSP00000290866.4:n.*689T=
ENST00000290866.9:c.*689T=	ENSP00000290866.4:n.*689T=
ENST00000428043.5:c.*1032T=	ENSP00000397593.2:n.*1032T=
ENST00000577647.2:c.1969+1070T=	ENSP00000464149.1:n.1969+1070T=
NM_000789.3:c.*689T=	NP_000780.1:n.*689T=
NM_001178057.1:c.*689T=	NP_001171528.1:n.*689T=
NM_152830.2:c.*689T=	NP_690043.1:n.*689T=
XM_005257110.1:c.*689T=	XP_005257167.1:n.*689T=
XM_006721737.2:c.*689T=	XP_006721800.2:n.*689T=
NM_000789.4:c.*689T= MANE Select	NP_000780.1:n.*689T=
NM_001178057.2:c.*689T=	NP_001171528.1:n.*689T=
NM_152830.3:c.*689T=	NP_690043.1:n.*689T=
NM_001382700.1:c.*689T=	NP_001369629.1:n.*689T=
NM_001382701.1:c.*689T=	NP_001369630.1:n.*689T=
NM_001382702.1:c.*689T=	NP_001369631.1:n.*689T=
NR_168483.1:n.2988T=