Canonical Allele Identifier: CA2269940201

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477892A= , CM000679.2:g.63477892A=	GRCh38
NC_000017.10:g.61555253A= , CM000679.1:g.61555253A=	GRCh37
NC_000017.9:g.58908985A=	NCBI36
NG_011648.1:g.5820A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.250-39A= MANE Select	ENSP00000290866.4:n.250-39A=
ENST00000290866.9:c.250-39A=	ENSP00000290866.4:n.250-39A=
ENST00000428043.5:c.250-39A=	ENSP00000397593.2:n.250-39A=
ENST00000579462.1:n.275-39A=
ENST00000580318.1:n.400A=
ENST00000582627.1:c.250-39A=	ENSP00000462280.1:n.250-39A=
ENST00000582678.5:c.250-39A=	ENSP00000462995.1:n.250-39A=
ENST00000583336.5:n.284-39A=
ENST00000584529.5:n.284-39A=
NM_000789.3:c.250-39A=	NP_000780.1:n.250-39A=
XM_005257110.1:c.-206-39A=	XP_005257167.1:n.-206-39A=
NM_000789.4:c.250-39A= MANE Select	NP_000780.1:n.250-39A=
NM_001382700.1:c.15-39A=	NP_001369629.1:n.15-39A=
NM_001382701.1:c.-365-39A=	NP_001369630.1:n.-365-39A=