Canonical Allele Identifier: CA2269946078

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488951T= , CM000679.2:g.63488951T=	GRCh38
NC_000017.10:g.61566312T= , CM000679.1:g.61566312T=	GRCh37
NC_000017.9:g.58920044T=	NCBI36
NG_011648.1:g.16879T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2460T= MANE Select	ENSP00000290866.4:p.Asp820=
ENST00000290863.10:c.738T=	ENSP00000290863.6:p.Asp246=
ENST00000290866.9:c.2460T=	ENSP00000290866.4:p.Asp820=
ENST00000413513.7:c.738T=	ENSP00000392247.3:p.Asp246=
ENST00000428043.5:c.2460T=	ENSP00000397593.2:p.Asp820=
ENST00000577647.2:c.738T=	ENSP00000464149.1:p.Asp246=
ENST00000578839.5:c.*519+160T=	ENSP00000462110.2:n.*519+160T=
ENST00000579204.1:c.719T=	ENSP00000464629.1:n.719T=
ENST00000579314.5:c.*189T=	ENSP00000462599.1:n.*189T=
ENST00000582005.5:c.*380T=	ENSP00000462002.1:n.*380T=
ENST00000582761.1:c.228T=	ENSP00000462909.1:p.Asp76=
ENST00000584865.5:n.406T=
NM_000789.3:c.2460T=	NP_000780.1:p.Asp820=
NM_001178057.1:c.738T=	NP_001171528.1:p.Asp246=
NM_152830.2:c.738T=	NP_690043.1:p.Asp246=
XM_005257110.1:c.1911T=	XP_005257167.1:p.Asp637=
XM_006721737.2:c.798T=	XP_006721800.2:p.Asp266=
XM_006721737.3:c.798T=	XP_006721800.2:p.Asp266=
NM_000789.4:c.2460T= MANE Select	NP_000780.1:p.Asp820=
NM_001178057.2:c.738T=	NP_001171528.1:p.Asp246=
NM_152830.3:c.738T=	NP_690043.1:p.Asp246=
NM_001382700.1:c.1893T=	NP_001369629.1:p.Asp631=
NM_001382701.1:c.1608T=	NP_001369630.1:p.Asp536=
NM_001382702.1:c.379+160T=	NP_001369631.1:n.379+160T=
NR_168483.1:n.838T=