Canonical Allele Identifier: CA2269949770

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496841A= , CM000679.2:g.63496841A=	GRCh38
NC_000017.10:g.61574202A= , CM000679.1:g.61574202A=	GRCh37
NC_000017.9:g.58927934A=	NCBI36
NG_011648.1:g.24769A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3547A= MANE Select	ENSP00000290866.4:p.Met1183=
ENST00000290863.10:c.1825A=	ENSP00000290863.6:p.Met609=
ENST00000290866.9:c.3547A=	ENSP00000290866.4:p.Met1183=
ENST00000413513.7:c.1702A=	ENSP00000392247.3:p.Met568=
ENST00000428043.5:c.3547A=	ENSP00000397593.2:p.Met1183=
ENST00000577418.5:n.557A=
ENST00000577647.2:c.1825A=	ENSP00000464149.1:p.Met609=
ENST00000578839.5:c.*1302A=	ENSP00000462110.2:n.*1302A=
ENST00000579314.5:c.*1276A=	ENSP00000462599.1:n.*1276A=
ENST00000579409.1:c.234A=
ENST00000582244.1:n.421A=
NM_000789.3:c.3547A=	NP_000780.1:p.Met1183=
NM_001178057.1:c.1702A=	NP_001171528.1:p.Met568=
NM_152830.2:c.1825A=	NP_690043.1:p.Met609=
XM_005257110.1:c.2998A=	XP_005257167.1:p.Met1000=
XM_006721737.2:c.1885A=	XP_006721800.2:p.Met629=
XM_006721737.3:c.1885A=	XP_006721800.2:p.Met629=
NM_000789.4:c.3547A= MANE Select	NP_000780.1:p.Met1183=
NM_001178057.2:c.1702A=	NP_001171528.1:p.Met568=
NM_152830.3:c.1825A=	NP_690043.1:p.Met609=
NM_001382700.1:c.2980A=	NP_001369629.1:p.Met994=
NM_001382701.1:c.2695A=	NP_001369630.1:p.Met899=
NM_001382702.1:c.1162A=	NP_001369631.1:p.Met388=
NR_168483.1:n.1925A=