Canonical Allele Identifier: CA2269940030

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477579T= , CM000679.2:g.63477579T=	GRCh38
NC_000017.10:g.61554940T= , CM000679.1:g.61554940T=	GRCh37
NC_000017.9:g.58908672T=	NCBI36
NG_011648.1:g.5507T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.249+236T= MANE Select	ENSP00000290866.4:n.249+236T=
ENST00000290866.9:c.249+236T=	ENSP00000290866.4:n.249+236T=
ENST00000428043.5:c.249+236T=	ENSP00000397593.2:n.249+236T=
ENST00000579462.1:n.274+236T=
ENST00000580318.1:n.87T=
ENST00000582627.1:c.38T=	ENSP00000462280.1:p.Phe13=
ENST00000582678.5:c.249+236T=	ENSP00000462995.1:n.249+236T=
ENST00000583336.5:n.283+236T=
ENST00000584529.5:n.283+236T=
NM_000789.3:c.249+236T=	NP_000780.1:n.249+236T=
XM_005257110.1:c.-207+236T=	XP_005257167.1:n.-207+236T=
NM_000789.4:c.249+236T= MANE Select	NP_000780.1:n.249+236T=
NM_001382700.1:c.14+236T=	NP_001369629.1:n.14+236T=
NM_001382701.1:c.-366+236T=	NP_001369630.1:n.-366+236T=