Canonical Allele Identifier: CA2269949826

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496947A= , CM000679.2:g.63496947A=	GRCh38
NC_000017.10:g.61574308A= , CM000679.1:g.61574308A=	GRCh37
NC_000017.9:g.58928040A=	NCBI36
NG_011648.1:g.24875A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3653A= MANE Select	ENSP00000290866.4:p.Lys1218=
ENST00000290863.10:c.1931A=	ENSP00000290863.6:p.Lys644=
ENST00000290866.9:c.3653A=	ENSP00000290866.4:p.Lys1218=
ENST00000413513.7:c.1808A=	ENSP00000392247.3:p.Lys603=
ENST00000428043.5:c.3653A=	ENSP00000397593.2:p.Lys1218=
ENST00000577418.5:n.663A=
ENST00000577647.2:c.1931A=	ENSP00000464149.1:p.Lys644=
ENST00000578839.5:c.*1408A=	ENSP00000462110.2:n.*1408A=
ENST00000579314.5:c.*1382A=	ENSP00000462599.1:n.*1382A=
ENST00000579409.1:c.340A=
ENST00000582244.1:n.527A=
NM_000789.3:c.3653A=	NP_000780.1:p.Lys1218=
NM_001178057.1:c.1808A=	NP_001171528.1:p.Lys603=
NM_152830.2:c.1931A=	NP_690043.1:p.Lys644=
XM_005257110.1:c.3104A=	XP_005257167.1:p.Lys1035=
XM_006721737.2:c.1991A=	XP_006721800.2:p.Lys664=
XM_006721737.3:c.1991A=	XP_006721800.2:p.Lys664=
NM_000789.4:c.3653A= MANE Select	NP_000780.1:p.Lys1218=
NM_001178057.2:c.1808A=	NP_001171528.1:p.Lys603=
NM_152830.3:c.1931A=	NP_690043.1:p.Lys644=
NM_001382700.1:c.3086A=	NP_001369629.1:p.Lys1029=
NM_001382701.1:c.2801A=	NP_001369630.1:p.Lys934=
NM_001382702.1:c.1268A=	NP_001369631.1:p.Lys423=
NR_168483.1:n.2031A=