Canonical Allele Identifier: CA2269945988

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488772C= , CM000679.2:g.63488772C=	GRCh38
NC_000017.10:g.61566133C= , CM000679.1:g.61566133C=	GRCh37
NC_000017.9:g.58919865C=	NCBI36
NG_011648.1:g.16700C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2430C= MANE Select	ENSP00000290866.4:p.Asn810=
ENST00000290863.10:c.708C=	ENSP00000290863.6:p.Asn236=
ENST00000290866.9:c.2430C=	ENSP00000290866.4:p.Asn810=
ENST00000413513.7:c.708C=	ENSP00000392247.3:p.Asn236=
ENST00000428043.5:c.2430C=	ENSP00000397593.2:p.Asn810=
ENST00000577647.2:c.708C=	ENSP00000464149.1:p.Asn236=
ENST00000578839.5:c.*500C=	ENSP00000462110.2:n.*500C=
ENST00000579204.1:c.689C=	ENSP00000464629.1:n.689C=
ENST00000579314.5:c.*159C=	ENSP00000462599.1:n.*159C=
ENST00000582005.5:c.*350C=	ENSP00000462002.1:n.*350C=
ENST00000582761.1:c.198C=	ENSP00000462909.1:p.Asn66=
ENST00000584865.5:n.376C=
NM_000789.3:c.2430C=	NP_000780.1:p.Asn810=
NM_001178057.1:c.708C=	NP_001171528.1:p.Asn236=
NM_152830.2:c.708C=	NP_690043.1:p.Asn236=
XM_005257110.1:c.1881C=	XP_005257167.1:p.Asn627=
XM_006721737.2:c.768C=	XP_006721800.2:p.Asn256=
XM_006721737.3:c.768C=	XP_006721800.2:p.Asn256=
NM_000789.4:c.2430C= MANE Select	NP_000780.1:p.Asn810=
NM_001178057.2:c.708C=	NP_001171528.1:p.Asn236=
NM_152830.3:c.708C=	NP_690043.1:p.Asn236=
NM_001382700.1:c.1863C=	NP_001369629.1:p.Asn621=
NM_001382701.1:c.1578C=	NP_001369630.1:p.Asn526=
NM_001382702.1:c.360C=	NP_001369631.1:p.Asn120=
NR_168483.1:n.808C=