Canonical Allele Identifier: CA2269945989

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488774A= , CM000679.2:g.63488774A=	GRCh38
NC_000017.10:g.61566135A= , CM000679.1:g.61566135A=	GRCh37
NC_000017.9:g.58919867A=	NCBI36
NG_011648.1:g.16702A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2432A= MANE Select	ENSP00000290866.4:p.Gln811=
ENST00000290863.10:c.710A=	ENSP00000290863.6:p.Gln237=
ENST00000290866.9:c.2432A=	ENSP00000290866.4:p.Gln811=
ENST00000413513.7:c.710A=	ENSP00000392247.3:p.Gln237=
ENST00000428043.5:c.2432A=	ENSP00000397593.2:p.Gln811=
ENST00000577647.2:c.710A=	ENSP00000464149.1:p.Gln237=
ENST00000578839.5:c.*502A=	ENSP00000462110.2:n.*502A=
ENST00000579204.1:c.691A=	ENSP00000464629.1:n.691A=
ENST00000579314.5:c.*161A=	ENSP00000462599.1:n.*161A=
ENST00000582005.5:c.*352A=	ENSP00000462002.1:n.*352A=
ENST00000582761.1:c.200A=	ENSP00000462909.1:p.Gln67=
ENST00000584865.5:n.378A=
NM_000789.3:c.2432A=	NP_000780.1:p.Gln811=
NM_001178057.1:c.710A=	NP_001171528.1:p.Gln237=
NM_152830.2:c.710A=	NP_690043.1:p.Gln237=
XM_005257110.1:c.1883A=	XP_005257167.1:p.Gln628=
XM_006721737.2:c.770A=	XP_006721800.2:p.Gln257=
XM_006721737.3:c.770A=	XP_006721800.2:p.Gln257=
NM_000789.4:c.2432A= MANE Select	NP_000780.1:p.Gln811=
NM_001178057.2:c.710A=	NP_001171528.1:p.Gln237=
NM_152830.3:c.710A=	NP_690043.1:p.Gln237=
NM_001382700.1:c.1865A=	NP_001369629.1:p.Gln622=
NM_001382701.1:c.1580A=	NP_001369630.1:p.Gln527=
NM_001382702.1:c.362A=	NP_001369631.1:p.Gln121=
NR_168483.1:n.810A=