Canonical Allele Identifier: CA2269950005

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497214G= , CM000679.2:g.63497214G=	GRCh38
NC_000017.10:g.61574575G= , CM000679.1:g.61574575G=	GRCh37
NC_000017.9:g.58928307G=	NCBI36
NG_011648.1:g.25142G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3769G= MANE Select	ENSP00000290866.4:p.Val1257=
ENST00000290863.10:c.2047G=	ENSP00000290863.6:p.Val683=
ENST00000290866.9:c.3769G=	ENSP00000290866.4:p.Val1257=
ENST00000413513.7:c.1924G=	ENSP00000392247.3:p.Val642=
ENST00000428043.5:c.*191G=	ENSP00000397593.2:n.*191G=
ENST00000577647.2:c.1969+229G=	ENSP00000464149.1:n.1969+229G=
ENST00000578839.5:c.*1524G=	ENSP00000462110.2:n.*1524G=
ENST00000579314.5:c.*1498G=	ENSP00000462599.1:n.*1498G=
NM_000789.3:c.3769G=	NP_000780.1:p.Val1257=
NM_001178057.1:c.1924G=	NP_001171528.1:p.Val642=
NM_152830.2:c.2047G=	NP_690043.1:p.Val683=
XM_005257110.1:c.3220G=	XP_005257167.1:p.Val1074=
XM_006721737.2:c.2107G=	XP_006721800.2:p.Val703=
XM_006721737.3:c.2107G=	XP_006721800.2:p.Val703=
NM_000789.4:c.3769G= MANE Select	NP_000780.1:p.Val1257=
NM_001178057.2:c.1924G=	NP_001171528.1:p.Val642=
NM_152830.3:c.2047G=	NP_690043.1:p.Val683=
NM_001382700.1:c.3202G=	NP_001369629.1:p.Val1068=
NM_001382701.1:c.2917G=	NP_001369630.1:p.Val973=
NM_001382702.1:c.1384G=	NP_001369631.1:p.Val462=
NR_168483.1:n.2147G=