Canonical Allele Identifier: CA2269940313

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478110G= , CM000679.2:g.63478110G=	GRCh38
NC_000017.10:g.61555471G= , CM000679.1:g.61555471G=	GRCh37
NC_000017.9:g.58909203G=	NCBI36
NG_011648.1:g.6038G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.417+12G= MANE Select	ENSP00000290866.4:n.417+12G=
ENST00000290866.9:c.417+12G=	ENSP00000290866.4:n.417+12G=
ENST00000428043.5:c.417+12G=	ENSP00000397593.2:n.417+12G=
ENST00000579462.1:n.454G=
ENST00000580318.1:n.606+12G=
ENST00000582627.1:c.417+12G=	ENSP00000462280.1:n.417+12G=
ENST00000582678.5:c.417+12G=	ENSP00000462995.1:n.417+12G=
ENST00000583336.5:n.451+12G=
ENST00000584529.5:n.451+12G=
NM_000789.3:c.417+12G=	NP_000780.1:n.417+12G=
XM_005257110.1:c.-39+12G=	XP_005257167.1:n.-39+12G=
NM_000789.4:c.417+12G= MANE Select	NP_000780.1:n.417+12G=
NM_001382700.1:c.182+12G=	NP_001369629.1:n.182+12G=
NM_001382701.1:c.-198+12G=	NP_001369630.1:n.-198+12G=