Canonical Allele Identifier: CA2269941744

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63480951A= , CM000679.2:g.63480951A=	GRCh38
NC_000017.10:g.61558312A= , CM000679.1:g.61558312A=	GRCh37
NC_000017.9:g.58912044A=	NCBI36
NG_011648.1:g.8879A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.848-140A= MANE Select	ENSP00000290866.4:n.848-140A=
ENST00000290866.9:c.848-140A=	ENSP00000290866.4:n.848-140A=
ENST00000428043.5:c.848-140A=	ENSP00000397593.2:n.848-140A=
ENST00000582627.1:c.848-140A=	ENSP00000462280.1:n.848-140A=
ENST00000582678.5:c.*247-140A=	ENSP00000462995.1:n.*247-140A=
ENST00000584529.5:n.882-140A=
NM_000789.3:c.848-140A=	NP_000780.1:n.848-140A=
XM_005257110.1:c.299-140A=	XP_005257167.1:n.299-140A=
NM_000789.4:c.848-140A= MANE Select	NP_000780.1:n.848-140A=
NM_001382700.1:c.375-140A=	NP_001369629.1:n.375-140A=
NM_001382701.1:c.-5-140A=	NP_001369630.1:n.-5-140A=