Canonical Allele Identifier: CA2269945952

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488703G= , CM000679.2:g.63488703G=	GRCh38
NC_000017.10:g.61566064G= , CM000679.1:g.61566064G=	GRCh37
NC_000017.9:g.58919796G=	NCBI36
NG_011648.1:g.16631G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2361G= MANE Select	ENSP00000290866.4:p.Trp787=
ENST00000290863.10:c.639G=	ENSP00000290863.6:p.Trp213=
ENST00000290866.9:c.2361G=	ENSP00000290866.4:p.Trp787=
ENST00000413513.7:c.639G=	ENSP00000392247.3:p.Trp213=
ENST00000428043.5:c.2361G=	ENSP00000397593.2:p.Trp787=
ENST00000577647.2:c.639G=	ENSP00000464149.1:p.Trp213=
ENST00000578839.5:c.*431G=	ENSP00000462110.2:n.*431G=
ENST00000579204.1:c.620G=	ENSP00000464629.1:n.620G=
ENST00000579314.5:c.*90G=	ENSP00000462599.1:n.*90G=
ENST00000582005.5:c.*281G=	ENSP00000462002.1:n.*281G=
ENST00000582761.1:c.129G=	ENSP00000462909.1:p.Trp43=
ENST00000584865.5:n.307G=
NM_000789.3:c.2361G=	NP_000780.1:p.Trp787=
NM_001178057.1:c.639G=	NP_001171528.1:p.Trp213=
NM_152830.2:c.639G=	NP_690043.1:p.Trp213=
XM_005257110.1:c.1812G=	XP_005257167.1:p.Trp604=
XM_006721737.2:c.699G=	XP_006721800.2:p.Trp233=
XM_006721737.3:c.699G=	XP_006721800.2:p.Trp233=
NM_000789.4:c.2361G= MANE Select	NP_000780.1:p.Trp787=
NM_001178057.2:c.639G=	NP_001171528.1:p.Trp213=
NM_152830.3:c.639G=	NP_690043.1:p.Trp213=
NM_001382700.1:c.1794G=	NP_001369629.1:p.Trp598=
NM_001382701.1:c.1509G=	NP_001369630.1:p.Trp503=
NM_001382702.1:c.291G=	NP_001369631.1:p.Trp97=
NR_168483.1:n.739G=