Canonical Allele Identifier: CA2269940300

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478088A= , CM000679.2:g.63478088A=	GRCh38
NC_000017.10:g.61555449A= , CM000679.1:g.61555449A=	GRCh37
NC_000017.9:g.58909181A=	NCBI36
NG_011648.1:g.6016A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.407A= MANE Select	ENSP00000290866.4:p.Lys136=
ENST00000290866.9:c.407A=	ENSP00000290866.4:p.Lys136=
ENST00000428043.5:c.407A=	ENSP00000397593.2:p.Lys136=
ENST00000579462.1:n.432A=
ENST00000580318.1:n.596A=
ENST00000582627.1:c.407A=	ENSP00000462280.1:p.Lys136=
ENST00000582678.5:c.407A=	ENSP00000462995.1:p.Lys136=
ENST00000583336.5:n.441A=
ENST00000584529.5:n.441A=
NM_000789.3:c.407A=	NP_000780.1:p.Lys136=
XM_005257110.1:c.-49A=	XP_005257167.1:n.-49A=
NM_000789.4:c.407A= MANE Select	NP_000780.1:p.Lys136=
NM_001382700.1:c.172A=	NP_001369629.1:p.Ser58=
NM_001382701.1:c.-208A=	NP_001369630.1:n.-208A=