Canonical Allele Identifier: CA2269940302

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478091G= , CM000679.2:g.63478091G=	GRCh38
NC_000017.10:g.61555452G= , CM000679.1:g.61555452G=	GRCh37
NC_000017.9:g.58909184G=	NCBI36
NG_011648.1:g.6019G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.410G= MANE Select	ENSP00000290866.4:p.Arg137=
ENST00000290866.9:c.410G=	ENSP00000290866.4:p.Arg137=
ENST00000428043.5:c.410G=	ENSP00000397593.2:p.Arg137=
ENST00000579462.1:n.435G=
ENST00000580318.1:n.599G=
ENST00000582627.1:c.410G=	ENSP00000462280.1:p.Arg137=
ENST00000582678.5:c.410G=	ENSP00000462995.1:p.Arg137=
ENST00000583336.5:n.444G=
ENST00000584529.5:n.444G=
NM_000789.3:c.410G=	NP_000780.1:p.Arg137=
XM_005257110.1:c.-46G=	XP_005257167.1:n.-46G=
NM_000789.4:c.410G= MANE Select	NP_000780.1:p.Arg137=
NM_001382700.1:c.175G=	NP_001369629.1:p.Gly59=
NM_001382701.1:c.-205G=	NP_001369630.1:n.-205G=