Canonical Allele Identifier: CA2269940298

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478086T= , CM000679.2:g.63478086T=	GRCh38
NC_000017.10:g.61555447T= , CM000679.1:g.61555447T=	GRCh37
NC_000017.9:g.58909179T=	NCBI36
NG_011648.1:g.6014T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.405T= MANE Select	ENSP00000290866.4:p.Ala135=
ENST00000290866.9:c.405T=	ENSP00000290866.4:p.Ala135=
ENST00000428043.5:c.405T=	ENSP00000397593.2:p.Ala135=
ENST00000579462.1:n.430T=
ENST00000580318.1:n.594T=
ENST00000582627.1:c.405T=	ENSP00000462280.1:p.Ala135=
ENST00000582678.5:c.405T=	ENSP00000462995.1:p.Ala135=
ENST00000583336.5:n.439T=
ENST00000584529.5:n.439T=
NM_000789.3:c.405T=	NP_000780.1:p.Ala135=
XM_005257110.1:c.-51T=	XP_005257167.1:n.-51T=
NM_000789.4:c.405T= MANE Select	NP_000780.1:p.Ala135=
NM_001382700.1:c.170T=	NP_001369629.1:p.Leu57=
NM_001382701.1:c.-210T=	NP_001369630.1:n.-210T=