Canonical Allele Identifier: CA2269940285

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478059C= , CM000679.2:g.63478059C=	GRCh38
NC_000017.10:g.61555420C= , CM000679.1:g.61555420C=	GRCh37
NC_000017.9:g.58909152C=	NCBI36
NG_011648.1:g.5987C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.378C= MANE Select	ENSP00000290866.4:p.Thr126=
ENST00000290866.9:c.378C=	ENSP00000290866.4:p.Thr126=
ENST00000428043.5:c.378C=	ENSP00000397593.2:p.Thr126=
ENST00000579462.1:n.403C=
ENST00000580318.1:n.567C=
ENST00000582627.1:c.378C=	ENSP00000462280.1:p.Thr126=
ENST00000582678.5:c.378C=	ENSP00000462995.1:p.Thr126=
ENST00000583336.5:n.412C=
ENST00000584529.5:n.412C=
NM_000789.3:c.378C=	NP_000780.1:p.Thr126=
XM_005257110.1:c.-78C=	XP_005257167.1:n.-78C=
NM_000789.4:c.378C= MANE Select	NP_000780.1:p.Thr126=
NM_001382700.1:c.143C=	NP_001369629.1:p.Pro48=
NM_001382701.1:c.-237C=	NP_001369630.1:n.-237C=