Canonical Allele Identifier: CA2269945066

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487011A= , CM000679.2:g.63487011A=	GRCh38
NC_000017.10:g.61564372A= , CM000679.1:g.61564372A=	GRCh37
NC_000017.9:g.58918104A=	NCBI36
NG_011648.1:g.14939A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2243A= MANE Select	ENSP00000290866.4:p.Glu748=
ENST00000290863.10:c.521A=	ENSP00000290863.6:p.Glu174=
ENST00000290866.9:c.2243A=	ENSP00000290866.4:p.Glu748=
ENST00000413513.7:c.521A=	ENSP00000392247.3:p.Glu174=
ENST00000428043.5:c.2243A=	ENSP00000397593.2:p.Glu748=
ENST00000577647.2:c.521A=	ENSP00000464149.1:p.Glu174=
ENST00000578839.5:c.*313A=	ENSP00000462110.2:n.*313A=
ENST00000579204.1:c.424A=	ENSP00000464629.1:n.424A=
ENST00000579314.5:c.521A=	ENSP00000462599.1:p.Glu174=
ENST00000579726.5:c.805A=
ENST00000582005.5:c.*163A=	ENSP00000462002.1:n.*163A=
ENST00000582761.1:c.11A=	ENSP00000462909.1:p.Glu4=
ENST00000584865.5:n.189A=
NM_000789.3:c.2243A=	NP_000780.1:p.Glu748=
NM_001178057.1:c.521A=	NP_001171528.1:p.Glu174=
NM_152830.2:c.521A=	NP_690043.1:p.Glu174=
XM_005257110.1:c.1694A=	XP_005257167.1:p.Glu565=
XM_006721737.2:c.581A=	XP_006721800.2:p.Glu194=
XM_006721737.3:c.581A=	XP_006721800.2:p.Glu194=
NM_000789.4:c.2243A= MANE Select	NP_000780.1:p.Glu748=
NM_001178057.2:c.521A=	NP_001171528.1:p.Glu174=
NM_152830.3:c.521A=	NP_690043.1:p.Glu174=
NM_001382700.1:c.1676A=	NP_001369629.1:p.Glu559=
NM_001382701.1:c.1391A=	NP_001369630.1:p.Glu464=
NM_001382702.1:c.173A=	NP_001369631.1:p.Glu58=
NR_168483.1:n.543A=