Canonical Allele Identifier: CA2269949825

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496946A= , CM000679.2:g.63496946A=	GRCh38
NC_000017.10:g.61574307A= , CM000679.1:g.61574307A=	GRCh37
NC_000017.9:g.58928039A=	NCBI36
NG_011648.1:g.24874A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3652A= MANE Select	ENSP00000290866.4:p.Lys1218=
ENST00000290863.10:c.1930A=	ENSP00000290863.6:p.Lys644=
ENST00000290866.9:c.3652A=	ENSP00000290866.4:p.Lys1218=
ENST00000413513.7:c.1807A=	ENSP00000392247.3:p.Lys603=
ENST00000428043.5:c.3652A=	ENSP00000397593.2:p.Lys1218=
ENST00000577418.5:n.662A=
ENST00000577647.2:c.1930A=	ENSP00000464149.1:p.Lys644=
ENST00000578839.5:c.*1407A=	ENSP00000462110.2:n.*1407A=
ENST00000579314.5:c.*1381A=	ENSP00000462599.1:n.*1381A=
ENST00000579409.1:c.339A=
ENST00000582244.1:n.526A=
NM_000789.3:c.3652A=	NP_000780.1:p.Lys1218=
NM_001178057.1:c.1807A=	NP_001171528.1:p.Lys603=
NM_152830.2:c.1930A=	NP_690043.1:p.Lys644=
XM_005257110.1:c.3103A=	XP_005257167.1:p.Lys1035=
XM_006721737.2:c.1990A=	XP_006721800.2:p.Lys664=
XM_006721737.3:c.1990A=	XP_006721800.2:p.Lys664=
NM_000789.4:c.3652A= MANE Select	NP_000780.1:p.Lys1218=
NM_001178057.2:c.1807A=	NP_001171528.1:p.Lys603=
NM_152830.3:c.1930A=	NP_690043.1:p.Lys644=
NM_001382700.1:c.3085A=	NP_001369629.1:p.Lys1029=
NM_001382701.1:c.2800A=	NP_001369630.1:p.Lys934=
NM_001382702.1:c.1267A=	NP_001369631.1:p.Lys423=
NR_168483.1:n.2030A=