Canonical Allele Identifier: CA2269944891

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486707C= , CM000679.2:g.63486707C=	GRCh38
NC_000017.10:g.61564068C= , CM000679.1:g.61564068C=	GRCh37
NC_000017.9:g.58917800C=	NCBI36
NG_011648.1:g.14635C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2209C= MANE Select	ENSP00000290866.4:p.Leu737=
ENST00000290863.10:c.487C=	ENSP00000290863.6:p.Leu163=
ENST00000290866.9:c.2209C=	ENSP00000290866.4:p.Leu737=
ENST00000413513.7:c.487C=	ENSP00000392247.3:p.Leu163=
ENST00000428043.5:c.2209C=	ENSP00000397593.2:p.Leu737=
ENST00000577647.2:c.487C=	ENSP00000464149.1:p.Leu163=
ENST00000578839.5:c.*279C=	ENSP00000462110.2:n.*279C=
ENST00000579204.1:c.390C=	ENSP00000464629.1:n.390C=
ENST00000579314.5:c.487C=	ENSP00000462599.1:p.Leu163=
ENST00000579726.5:c.771C=
ENST00000582005.5:c.*129C=	ENSP00000462002.1:n.*129C=
NM_000789.3:c.2209C=	NP_000780.1:p.Leu737=
NM_001178057.1:c.487C=	NP_001171528.1:p.Leu163=
NM_152830.2:c.487C=	NP_690043.1:p.Leu163=
XM_005257110.1:c.1660C=	XP_005257167.1:p.Leu554=
XM_006721737.2:c.547C=	XP_006721800.2:p.Leu183=
XM_006721737.3:c.547C=	XP_006721800.2:p.Leu183=
NM_000789.4:c.2209C= MANE Select	NP_000780.1:p.Leu737=
NM_001178057.2:c.487C=	NP_001171528.1:p.Leu163=
NM_152830.3:c.487C=	NP_690043.1:p.Leu163=
NM_001382700.1:c.1642C=	NP_001369629.1:p.Leu548=
NM_001382701.1:c.1357C=	NP_001369630.1:p.Leu453=
NM_001382702.1:c.139C=	NP_001369631.1:p.Leu47=
NR_168483.1:n.509C=