Canonical Allele Identifier: CA2269945096

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487067G= , CM000679.2:g.63487067G=	GRCh38
NC_000017.10:g.61564428G= , CM000679.1:g.61564428G=	GRCh37
NC_000017.9:g.58918160G=	NCBI36
NG_011648.1:g.14995G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2299G= MANE Select	ENSP00000290866.4:p.Glu767=
ENST00000290863.10:c.577G=	ENSP00000290863.6:p.Glu193=
ENST00000290866.9:c.2299G=	ENSP00000290866.4:p.Glu767=
ENST00000413513.7:c.577G=	ENSP00000392247.3:p.Glu193=
ENST00000428043.5:c.2299G=	ENSP00000397593.2:p.Glu767=
ENST00000577647.2:c.577G=	ENSP00000464149.1:p.Glu193=
ENST00000578839.5:c.*369G=	ENSP00000462110.2:n.*369G=
ENST00000579204.1:c.480G=	ENSP00000464629.1:n.480G=
ENST00000579314.5:c.577G=	ENSP00000462599.1:p.Glu193=
ENST00000579726.5:c.861G=
ENST00000582005.5:c.*219G=	ENSP00000462002.1:n.*219G=
ENST00000582761.1:c.67G=	ENSP00000462909.1:p.Glu23=
ENST00000584865.5:n.245G=
NM_000789.3:c.2299G=	NP_000780.1:p.Glu767=
NM_001178057.1:c.577G=	NP_001171528.1:p.Glu193=
NM_152830.2:c.577G=	NP_690043.1:p.Glu193=
XM_005257110.1:c.1750G=	XP_005257167.1:p.Glu584=
XM_006721737.2:c.637G=	XP_006721800.2:p.Glu213=
XM_006721737.3:c.637G=	XP_006721800.2:p.Glu213=
NM_000789.4:c.2299G= MANE Select	NP_000780.1:p.Glu767=
NM_001178057.2:c.577G=	NP_001171528.1:p.Glu193=
NM_152830.3:c.577G=	NP_690043.1:p.Glu193=
NM_001382700.1:c.1732G=	NP_001369629.1:p.Glu578=
NM_001382701.1:c.1447G=	NP_001369630.1:p.Glu483=
NM_001382702.1:c.229G=	NP_001369631.1:p.Glu77=
NR_168483.1:n.599G=