Canonical Allele Identifier: CA2269950013

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497234C= , CM000679.2:g.63497234C=	GRCh38
NC_000017.10:g.61574595C= , CM000679.1:g.61574595C=	GRCh37
NC_000017.9:g.58928327C=	NCBI36
NG_011648.1:g.25162C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3789C= MANE Select	ENSP00000290866.4:p.Leu1263=
ENST00000290863.10:c.2067C=	ENSP00000290863.6:p.Leu689=
ENST00000290866.9:c.3789C=	ENSP00000290866.4:p.Leu1263=
ENST00000413513.7:c.1944C=	ENSP00000392247.3:p.Leu648=
ENST00000428043.5:c.*211C=	ENSP00000397593.2:n.*211C=
ENST00000577647.2:c.1969+249C=	ENSP00000464149.1:n.1969+249C=
ENST00000578839.5:c.*1544C=	ENSP00000462110.2:n.*1544C=
ENST00000579314.5:c.*1518C=	ENSP00000462599.1:n.*1518C=
NM_000789.3:c.3789C=	NP_000780.1:p.Leu1263=
NM_001178057.1:c.1944C=	NP_001171528.1:p.Leu648=
NM_152830.2:c.2067C=	NP_690043.1:p.Leu689=
XM_005257110.1:c.3240C=	XP_005257167.1:p.Leu1080=
XM_006721737.2:c.2127C=	XP_006721800.2:p.Leu709=
XM_006721737.3:c.2127C=	XP_006721800.2:p.Leu709=
NM_000789.4:c.3789C= MANE Select	NP_000780.1:p.Leu1263=
NM_001178057.2:c.1944C=	NP_001171528.1:p.Leu648=
NM_152830.3:c.2067C=	NP_690043.1:p.Leu689=
NM_001382700.1:c.3222C=	NP_001369629.1:p.Leu1074=
NM_001382701.1:c.2937C=	NP_001369630.1:p.Leu979=
NM_001382702.1:c.1404C=	NP_001369631.1:p.Leu468=
NR_168483.1:n.2167C=