Canonical Allele Identifier: CA2269949762

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496825G= , CM000679.2:g.63496825G=	GRCh38
NC_000017.10:g.61574186G= , CM000679.1:g.61574186G=	GRCh37
NC_000017.9:g.58927918G=	NCBI36
NG_011648.1:g.24753G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3531G= MANE Select	ENSP00000290866.4:p.Arg1177=
ENST00000290863.10:c.1809G=	ENSP00000290863.6:p.Arg603=
ENST00000290866.9:c.3531G=	ENSP00000290866.4:p.Arg1177=
ENST00000413513.7:c.1686G=	ENSP00000392247.3:p.Arg562=
ENST00000428043.5:c.3531G=	ENSP00000397593.2:p.Arg1177=
ENST00000577418.5:n.541G=
ENST00000577647.2:c.1809G=	ENSP00000464149.1:p.Arg603=
ENST00000578839.5:c.*1286G=	ENSP00000462110.2:n.*1286G=
ENST00000579314.5:c.*1260G=	ENSP00000462599.1:n.*1260G=
ENST00000579409.1:c.218G=
ENST00000582244.1:n.405G=
NM_000789.3:c.3531G=	NP_000780.1:p.Arg1177=
NM_001178057.1:c.1686G=	NP_001171528.1:p.Arg562=
NM_152830.2:c.1809G=	NP_690043.1:p.Arg603=
XM_005257110.1:c.2982G=	XP_005257167.1:p.Arg994=
XM_006721737.2:c.1869G=	XP_006721800.2:p.Arg623=
XM_006721737.3:c.1869G=	XP_006721800.2:p.Arg623=
NM_000789.4:c.3531G= MANE Select	NP_000780.1:p.Arg1177=
NM_001178057.2:c.1686G=	NP_001171528.1:p.Arg562=
NM_152830.3:c.1809G=	NP_690043.1:p.Arg603=
NM_001382700.1:c.2964G=	NP_001369629.1:p.Arg988=
NM_001382701.1:c.2679G=	NP_001369630.1:p.Arg893=
NM_001382702.1:c.1146G=	NP_001369631.1:p.Arg382=
NR_168483.1:n.1909G=