Canonical Allele Identifier: CA2269940248

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477985A= , CM000679.2:g.63477985A=	GRCh38
NC_000017.10:g.61555346A= , CM000679.1:g.61555346A=	GRCh37
NC_000017.9:g.58909078A=	NCBI36
NG_011648.1:g.5913A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.304A= MANE Select	ENSP00000290866.4:p.Lys102=
ENST00000290866.9:c.304A=	ENSP00000290866.4:p.Lys102=
ENST00000428043.5:c.304A=	ENSP00000397593.2:p.Lys102=
ENST00000579462.1:n.329A=
ENST00000580318.1:n.493A=
ENST00000582627.1:c.304A=	ENSP00000462280.1:p.Lys102=
ENST00000582678.5:c.304A=	ENSP00000462995.1:p.Lys102=
ENST00000583336.5:n.338A=
ENST00000584529.5:n.338A=
NM_000789.3:c.304A=	NP_000780.1:p.Lys102=
XM_005257110.1:c.-152A=	XP_005257167.1:n.-152A=
NM_000789.4:c.304A= MANE Select	NP_000780.1:p.Lys102=
NM_001382700.1:c.69A=	NP_001369629.1:p.Pro23=
NM_001382701.1:c.-311A=	NP_001369630.1:n.-311A=