Canonical Allele Identifier: CA2269945054

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486991C= , CM000679.2:g.63486991C=	GRCh38
NC_000017.10:g.61564352C= , CM000679.1:g.61564352C=	GRCh37
NC_000017.9:g.58918084C=	NCBI36
NG_011648.1:g.14919C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2223C= MANE Select	ENSP00000290866.4:p.Asn741=
ENST00000290863.10:c.501C=	ENSP00000290863.6:p.Asn167=
ENST00000290866.9:c.2223C=	ENSP00000290866.4:p.Asn741=
ENST00000413513.7:c.501C=	ENSP00000392247.3:p.Asn167=
ENST00000428043.5:c.2223C=	ENSP00000397593.2:p.Asn741=
ENST00000577647.2:c.501C=	ENSP00000464149.1:p.Asn167=
ENST00000578839.5:c.*293C=	ENSP00000462110.2:n.*293C=
ENST00000579204.1:c.404C=	ENSP00000464629.1:n.404C=
ENST00000579314.5:c.501C=	ENSP00000462599.1:p.Asn167=
ENST00000579726.5:c.785C=
ENST00000582005.5:c.*143C=	ENSP00000462002.1:n.*143C=
ENST00000584865.5:n.169C=
NM_000789.3:c.2223C=	NP_000780.1:p.Asn741=
NM_001178057.1:c.501C=	NP_001171528.1:p.Asn167=
NM_152830.2:c.501C=	NP_690043.1:p.Asn167=
XM_005257110.1:c.1674C=	XP_005257167.1:p.Asn558=
XM_006721737.2:c.561C=	XP_006721800.2:p.Asn187=
XM_006721737.3:c.561C=	XP_006721800.2:p.Asn187=
NM_000789.4:c.2223C= MANE Select	NP_000780.1:p.Asn741=
NM_001178057.2:c.501C=	NP_001171528.1:p.Asn167=
NM_152830.3:c.501C=	NP_690043.1:p.Asn167=
NM_001382700.1:c.1656C=	NP_001369629.1:p.Asn552=
NM_001382701.1:c.1371C=	NP_001369630.1:p.Asn457=
NM_001382702.1:c.153C=	NP_001369631.1:p.Asn51=
NR_168483.1:n.523C=