Canonical Allele Identifier: CA2269939902

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477269C= , CM000679.2:g.63477269C=	GRCh38
NC_000017.10:g.61554630C= , CM000679.1:g.61554630C=	GRCh37
NC_000017.9:g.58908362C=	NCBI36
NG_011648.1:g.5197C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.175C= MANE Select	ENSP00000290866.4:p.Gln59=
ENST00000290866.9:c.175C=	ENSP00000290866.4:p.Gln59=
ENST00000428043.5:c.175C=	ENSP00000397593.2:p.Gln59=
ENST00000579462.1:n.200C=
ENST00000582678.5:c.175C=	ENSP00000462995.1:p.Gln59=
ENST00000583336.5:n.209C=
ENST00000584529.5:n.209C=
NM_000789.3:c.175C=	NP_000780.1:p.Gln59=
XM_005257110.1:c.-281C=	XP_005257167.1:n.-281C=
NM_000789.4:c.175C= MANE Select	NP_000780.1:p.Gln59=
NM_001382700.1:c.-61C=	NP_001369629.1:n.-61C=
NM_001382701.1:c.-440C=	NP_001369630.1:n.-440C=