Canonical Allele Identifier: CA2269945948

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488693T= , CM000679.2:g.63488693T=	GRCh38
NC_000017.10:g.61566054T= , CM000679.1:g.61566054T=	GRCh37
NC_000017.9:g.58919786T=	NCBI36
NG_011648.1:g.16621T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2351T= MANE Select	ENSP00000290866.4:p.Leu784=
ENST00000290863.10:c.629T=	ENSP00000290863.6:p.Leu210=
ENST00000290866.9:c.2351T=	ENSP00000290866.4:p.Leu784=
ENST00000413513.7:c.629T=	ENSP00000392247.3:p.Leu210=
ENST00000428043.5:c.2351T=	ENSP00000397593.2:p.Leu784=
ENST00000577647.2:c.629T=	ENSP00000464149.1:p.Leu210=
ENST00000578839.5:c.*421T=	ENSP00000462110.2:n.*421T=
ENST00000579204.1:c.610T=	ENSP00000464629.1:n.610T=
ENST00000579314.5:c.*80T=	ENSP00000462599.1:n.*80T=
ENST00000582005.5:c.*271T=	ENSP00000462002.1:n.*271T=
ENST00000582761.1:c.119T=	ENSP00000462909.1:p.Leu40=
ENST00000584865.5:n.297T=
NM_000789.3:c.2351T=	NP_000780.1:p.Leu784=
NM_001178057.1:c.629T=	NP_001171528.1:p.Leu210=
NM_152830.2:c.629T=	NP_690043.1:p.Leu210=
XM_005257110.1:c.1802T=	XP_005257167.1:p.Leu601=
XM_006721737.2:c.689T=	XP_006721800.2:p.Leu230=
XM_006721737.3:c.689T=	XP_006721800.2:p.Leu230=
NM_000789.4:c.2351T= MANE Select	NP_000780.1:p.Leu784=
NM_001178057.2:c.629T=	NP_001171528.1:p.Leu210=
NM_152830.3:c.629T=	NP_690043.1:p.Leu210=
NM_001382700.1:c.1784T=	NP_001369629.1:p.Leu595=
NM_001382701.1:c.1499T=	NP_001369630.1:p.Leu500=
NM_001382702.1:c.281T=	NP_001369631.1:p.Leu94=
NR_168483.1:n.729T=