Canonical Allele Identifier: CA2269945940

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488675G= , CM000679.2:g.63488675G=	GRCh38
NC_000017.10:g.61566036G= , CM000679.1:g.61566036G=	GRCh37
NC_000017.9:g.58919768G=	NCBI36
NG_011648.1:g.16603G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2333G= MANE Select	ENSP00000290866.4:p.Arg778=
ENST00000290863.10:c.611G=	ENSP00000290863.6:p.Arg204=
ENST00000290866.9:c.2333G=	ENSP00000290866.4:p.Arg778=
ENST00000413513.7:c.611G=	ENSP00000392247.3:p.Arg204=
ENST00000428043.5:c.2333G=	ENSP00000397593.2:p.Arg778=
ENST00000577647.2:c.611G=	ENSP00000464149.1:p.Arg204=
ENST00000578839.5:c.*403G=	ENSP00000462110.2:n.*403G=
ENST00000579204.1:c.592G=	ENSP00000464629.1:n.592G=
ENST00000579314.5:c.*62G=	ENSP00000462599.1:n.*62G=
ENST00000582005.5:c.*253G=	ENSP00000462002.1:n.*253G=
ENST00000582761.1:c.101G=	ENSP00000462909.1:p.Arg34=
ENST00000584865.5:n.279G=
NM_000789.3:c.2333G=	NP_000780.1:p.Arg778=
NM_001178057.1:c.611G=	NP_001171528.1:p.Arg204=
NM_152830.2:c.611G=	NP_690043.1:p.Arg204=
XM_005257110.1:c.1784G=	XP_005257167.1:p.Arg595=
XM_006721737.2:c.671G=	XP_006721800.2:p.Arg224=
XM_006721737.3:c.671G=	XP_006721800.2:p.Arg224=
NM_000789.4:c.2333G= MANE Select	NP_000780.1:p.Arg778=
NM_001178057.2:c.611G=	NP_001171528.1:p.Arg204=
NM_152830.3:c.611G=	NP_690043.1:p.Arg204=
NM_001382700.1:c.1766G=	NP_001369629.1:p.Arg589=
NM_001382701.1:c.1481G=	NP_001369630.1:p.Arg494=
NM_001382702.1:c.263G=	NP_001369631.1:p.Arg88=
NR_168483.1:n.711G=