Canonical Allele Identifier: CA2269945961

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488720A= , CM000679.2:g.63488720A=	GRCh38
NC_000017.10:g.61566081A= , CM000679.1:g.61566081A=	GRCh37
NC_000017.9:g.58919813A=	NCBI36
NG_011648.1:g.16648A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2378A= MANE Select	ENSP00000290866.4:p.Lys793=
ENST00000290863.10:c.656A=	ENSP00000290863.6:p.Lys219=
ENST00000290866.9:c.2378A=	ENSP00000290866.4:p.Lys793=
ENST00000413513.7:c.656A=	ENSP00000392247.3:p.Lys219=
ENST00000428043.5:c.2378A=	ENSP00000397593.2:p.Lys793=
ENST00000577647.2:c.656A=	ENSP00000464149.1:p.Lys219=
ENST00000578839.5:c.*448A=	ENSP00000462110.2:n.*448A=
ENST00000579204.1:c.637A=	ENSP00000464629.1:n.637A=
ENST00000579314.5:c.*107A=	ENSP00000462599.1:n.*107A=
ENST00000582005.5:c.*298A=	ENSP00000462002.1:n.*298A=
ENST00000582761.1:c.146A=	ENSP00000462909.1:p.Lys49=
ENST00000584865.5:n.324A=
NM_000789.3:c.2378A=	NP_000780.1:p.Lys793=
NM_001178057.1:c.656A=	NP_001171528.1:p.Lys219=
NM_152830.2:c.656A=	NP_690043.1:p.Lys219=
XM_005257110.1:c.1829A=	XP_005257167.1:p.Lys610=
XM_006721737.2:c.716A=	XP_006721800.2:p.Lys239=
XM_006721737.3:c.716A=	XP_006721800.2:p.Lys239=
NM_000789.4:c.2378A= MANE Select	NP_000780.1:p.Lys793=
NM_001178057.2:c.656A=	NP_001171528.1:p.Lys219=
NM_152830.3:c.656A=	NP_690043.1:p.Lys219=
NM_001382700.1:c.1811A=	NP_001369629.1:p.Lys604=
NM_001382701.1:c.1526A=	NP_001369630.1:p.Lys509=
NM_001382702.1:c.308A=	NP_001369631.1:p.Lys103=
NR_168483.1:n.756A=