Canonical Allele Identifier: CA2269945072

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487023G= , CM000679.2:g.63487023G=	GRCh38
NC_000017.10:g.61564384G= , CM000679.1:g.61564384G=	GRCh37
NC_000017.9:g.58918116G=	NCBI36
NG_011648.1:g.14951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2255G= MANE Select	ENSP00000290866.4:p.Ser752=
ENST00000290863.10:c.533G=	ENSP00000290863.6:p.Ser178=
ENST00000290866.9:c.2255G=	ENSP00000290866.4:p.Ser752=
ENST00000413513.7:c.533G=	ENSP00000392247.3:p.Ser178=
ENST00000428043.5:c.2255G=	ENSP00000397593.2:p.Ser752=
ENST00000577647.2:c.533G=	ENSP00000464149.1:p.Ser178=
ENST00000578839.5:c.*325G=	ENSP00000462110.2:n.*325G=
ENST00000579204.1:c.436G=	ENSP00000464629.1:n.436G=
ENST00000579314.5:c.533G=	ENSP00000462599.1:p.Ser178=
ENST00000579726.5:c.817G=
ENST00000582005.5:c.*175G=	ENSP00000462002.1:n.*175G=
ENST00000582761.1:c.23G=	ENSP00000462909.1:p.Ser8=
ENST00000584865.5:n.201G=
NM_000789.3:c.2255G=	NP_000780.1:p.Ser752=
NM_001178057.1:c.533G=	NP_001171528.1:p.Ser178=
NM_152830.2:c.533G=	NP_690043.1:p.Ser178=
XM_005257110.1:c.1706G=	XP_005257167.1:p.Ser569=
XM_006721737.2:c.593G=	XP_006721800.2:p.Ser198=
XM_006721737.3:c.593G=	XP_006721800.2:p.Ser198=
NM_000789.4:c.2255G= MANE Select	NP_000780.1:p.Ser752=
NM_001178057.2:c.533G=	NP_001171528.1:p.Ser178=
NM_152830.3:c.533G=	NP_690043.1:p.Ser178=
NM_001382700.1:c.1688G=	NP_001369629.1:p.Ser563=
NM_001382701.1:c.1403G=	NP_001369630.1:p.Ser468=
NM_001382702.1:c.185G=	NP_001369631.1:p.Ser62=
NR_168483.1:n.555G=