Canonical Allele Identifier: CA2269949752

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496801C= , CM000679.2:g.63496801C=	GRCh38
NC_000017.10:g.61574162C= , CM000679.1:g.61574162C=	GRCh37
NC_000017.9:g.58927894C=	NCBI36
NG_011648.1:g.24729C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3507C= MANE Select	ENSP00000290866.4:p.Thr1169=
ENST00000290863.10:c.1785C=	ENSP00000290863.6:p.Thr595=
ENST00000290866.9:c.3507C=	ENSP00000290866.4:p.Thr1169=
ENST00000413513.7:c.1662C=	ENSP00000392247.3:p.Thr554=
ENST00000428043.5:c.3507C=	ENSP00000397593.2:p.Thr1169=
ENST00000577418.5:n.517C=
ENST00000577647.2:c.1785C=	ENSP00000464149.1:p.Thr595=
ENST00000578839.5:c.*1262C=	ENSP00000462110.2:n.*1262C=
ENST00000579314.5:c.*1236C=	ENSP00000462599.1:n.*1236C=
ENST00000579409.1:c.194C=
ENST00000582244.1:n.381C=
NM_000789.3:c.3507C=	NP_000780.1:p.Thr1169=
NM_001178057.1:c.1662C=	NP_001171528.1:p.Thr554=
NM_152830.2:c.1785C=	NP_690043.1:p.Thr595=
XM_005257110.1:c.2958C=	XP_005257167.1:p.Thr986=
XM_006721737.2:c.1845C=	XP_006721800.2:p.Thr615=
XM_006721737.3:c.1845C=	XP_006721800.2:p.Thr615=
NM_000789.4:c.3507C= MANE Select	NP_000780.1:p.Thr1169=
NM_001178057.2:c.1662C=	NP_001171528.1:p.Thr554=
NM_152830.3:c.1785C=	NP_690043.1:p.Thr595=
NM_001382700.1:c.2940C=	NP_001369629.1:p.Thr980=
NM_001382701.1:c.2655C=	NP_001369630.1:p.Thr885=
NM_001382702.1:c.1122C=	NP_001369631.1:p.Thr374=
NR_168483.1:n.1885C=