Canonical Allele Identifier: CA2269945068

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487015C= , CM000679.2:g.63487015C=	GRCh38
NC_000017.10:g.61564376C= , CM000679.1:g.61564376C=	GRCh37
NC_000017.9:g.58918108C=	NCBI36
NG_011648.1:g.14943C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2247C= MANE Select	ENSP00000290866.4:p.Thr749=
ENST00000290863.10:c.525C=	ENSP00000290863.6:p.Thr175=
ENST00000290866.9:c.2247C=	ENSP00000290866.4:p.Thr749=
ENST00000413513.7:c.525C=	ENSP00000392247.3:p.Thr175=
ENST00000428043.5:c.2247C=	ENSP00000397593.2:p.Thr749=
ENST00000577647.2:c.525C=	ENSP00000464149.1:p.Thr175=
ENST00000578839.5:c.*317C=	ENSP00000462110.2:n.*317C=
ENST00000579204.1:c.428C=	ENSP00000464629.1:n.428C=
ENST00000579314.5:c.525C=	ENSP00000462599.1:p.Thr175=
ENST00000579726.5:c.809C=
ENST00000582005.5:c.*167C=	ENSP00000462002.1:n.*167C=
ENST00000582761.1:c.15C=	ENSP00000462909.1:p.Thr5=
ENST00000584865.5:n.193C=
NM_000789.3:c.2247C=	NP_000780.1:p.Thr749=
NM_001178057.1:c.525C=	NP_001171528.1:p.Thr175=
NM_152830.2:c.525C=	NP_690043.1:p.Thr175=
XM_005257110.1:c.1698C=	XP_005257167.1:p.Thr566=
XM_006721737.2:c.585C=	XP_006721800.2:p.Thr195=
XM_006721737.3:c.585C=	XP_006721800.2:p.Thr195=
NM_000789.4:c.2247C= MANE Select	NP_000780.1:p.Thr749=
NM_001178057.2:c.525C=	NP_001171528.1:p.Thr175=
NM_152830.3:c.525C=	NP_690043.1:p.Thr175=
NM_001382700.1:c.1680C=	NP_001369629.1:p.Thr560=
NM_001382701.1:c.1395C=	NP_001369630.1:p.Thr465=
NM_001382702.1:c.177C=	NP_001369631.1:p.Thr59=
NR_168483.1:n.547C=