Canonical Allele Identifier: CA2269950019

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497247G= , CM000679.2:g.63497247G=	GRCh38
NC_000017.10:g.61574608G= , CM000679.1:g.61574608G=	GRCh37
NC_000017.9:g.58928340G=	NCBI36
NG_011648.1:g.25175G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3802G= MANE Select	ENSP00000290866.4:p.Ala1268=
ENST00000290863.10:c.2080G=	ENSP00000290863.6:p.Ala694=
ENST00000290866.9:c.3802G=	ENSP00000290866.4:p.Ala1268=
ENST00000413513.7:c.1957G=	ENSP00000392247.3:p.Ala653=
ENST00000428043.5:c.*224G=	ENSP00000397593.2:n.*224G=
ENST00000577647.2:c.1969+262G=	ENSP00000464149.1:n.1969+262G=
ENST00000578839.5:c.*1557G=	ENSP00000462110.2:n.*1557G=
ENST00000579314.5:c.*1531G=	ENSP00000462599.1:n.*1531G=
NM_000789.3:c.3802G=	NP_000780.1:p.Ala1268=
NM_001178057.1:c.1957G=	NP_001171528.1:p.Ala653=
NM_152830.2:c.2080G=	NP_690043.1:p.Ala694=
XM_005257110.1:c.3253G=	XP_005257167.1:p.Ala1085=
XM_006721737.2:c.2140G=	XP_006721800.2:p.Ala714=
XM_006721737.3:c.2140G=	XP_006721800.2:p.Ala714=
NM_000789.4:c.3802G= MANE Select	NP_000780.1:p.Ala1268=
NM_001178057.2:c.1957G=	NP_001171528.1:p.Ala653=
NM_152830.3:c.2080G=	NP_690043.1:p.Ala694=
NM_001382700.1:c.3235G=	NP_001369629.1:p.Ala1079=
NM_001382701.1:c.2950G=	NP_001369630.1:p.Ala984=
NM_001382702.1:c.1417G=	NP_001369631.1:p.Ala473=
NR_168483.1:n.2180G=