Canonical Allele Identifier: CA2269946084

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488958G= , CM000679.2:g.63488958G=	GRCh38
NC_000017.10:g.61566319G= , CM000679.1:g.61566319G=	GRCh37
NC_000017.9:g.58920051G=	NCBI36
NG_011648.1:g.16886G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2467G= MANE Select	ENSP00000290866.4:p.Asp823=
ENST00000290863.10:c.745G=	ENSP00000290863.6:p.Asp249=
ENST00000290866.9:c.2467G=	ENSP00000290866.4:p.Asp823=
ENST00000413513.7:c.745G=	ENSP00000392247.3:p.Asp249=
ENST00000428043.5:c.2467G=	ENSP00000397593.2:p.Asp823=
ENST00000577647.2:c.745G=	ENSP00000464149.1:p.Asp249=
ENST00000578839.5:c.*519+167G=	ENSP00000462110.2:n.*519+167G=
ENST00000579204.1:c.726G=	ENSP00000464629.1:n.726G=
ENST00000579314.5:c.*196G=	ENSP00000462599.1:n.*196G=
ENST00000582005.5:c.*387G=	ENSP00000462002.1:n.*387G=
ENST00000582761.1:c.235G=	ENSP00000462909.1:p.Asp79=
ENST00000584865.5:n.413G=
NM_000789.3:c.2467G=	NP_000780.1:p.Asp823=
NM_001178057.1:c.745G=	NP_001171528.1:p.Asp249=
NM_152830.2:c.745G=	NP_690043.1:p.Asp249=
XM_005257110.1:c.1918G=	XP_005257167.1:p.Asp640=
XM_006721737.2:c.805G=	XP_006721800.2:p.Asp269=
XM_006721737.3:c.805G=	XP_006721800.2:p.Asp269=
NM_000789.4:c.2467G= MANE Select	NP_000780.1:p.Asp823=
NM_001178057.2:c.745G=	NP_001171528.1:p.Asp249=
NM_152830.3:c.745G=	NP_690043.1:p.Asp249=
NM_001382700.1:c.1900G=	NP_001369629.1:p.Asp634=
NM_001382701.1:c.1615G=	NP_001369630.1:p.Asp539=
NM_001382702.1:c.379+167G=	NP_001369631.1:n.379+167G=
NR_168483.1:n.845G=