Canonical Allele Identifier: CA2269945968

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488731G= , CM000679.2:g.63488731G=	GRCh38
NC_000017.10:g.61566092G= , CM000679.1:g.61566092G=	GRCh37
NC_000017.9:g.58919824G=	NCBI36
NG_011648.1:g.16659G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2389G= MANE Select	ENSP00000290866.4:p.Ala797=
ENST00000290863.10:c.667G=	ENSP00000290863.6:p.Ala223=
ENST00000290866.9:c.2389G=	ENSP00000290866.4:p.Ala797=
ENST00000413513.7:c.667G=	ENSP00000392247.3:p.Ala223=
ENST00000428043.5:c.2389G=	ENSP00000397593.2:p.Ala797=
ENST00000577647.2:c.667G=	ENSP00000464149.1:p.Ala223=
ENST00000578839.5:c.*459G=	ENSP00000462110.2:n.*459G=
ENST00000579204.1:c.648G=	ENSP00000464629.1:n.648G=
ENST00000579314.5:c.*118G=	ENSP00000462599.1:n.*118G=
ENST00000582005.5:c.*309G=	ENSP00000462002.1:n.*309G=
ENST00000582761.1:c.157G=	ENSP00000462909.1:p.Ala53=
ENST00000584865.5:n.335G=
NM_000789.3:c.2389G=	NP_000780.1:p.Ala797=
NM_001178057.1:c.667G=	NP_001171528.1:p.Ala223=
NM_152830.2:c.667G=	NP_690043.1:p.Ala223=
XM_005257110.1:c.1840G=	XP_005257167.1:p.Ala614=
XM_006721737.2:c.727G=	XP_006721800.2:p.Ala243=
XM_006721737.3:c.727G=	XP_006721800.2:p.Ala243=
NM_000789.4:c.2389G= MANE Select	NP_000780.1:p.Ala797=
NM_001178057.2:c.667G=	NP_001171528.1:p.Ala223=
NM_152830.3:c.667G=	NP_690043.1:p.Ala223=
NM_001382700.1:c.1822G=	NP_001369629.1:p.Ala608=
NM_001382701.1:c.1537G=	NP_001369630.1:p.Ala513=
NM_001382702.1:c.319G=	NP_001369631.1:p.Ala107=
NR_168483.1:n.767G=