Canonical Allele Identifier: CA2269945879

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488571T= , CM000679.2:g.63488571T=	GRCh38
NC_000017.10:g.61565932T= , CM000679.1:g.61565932T=	GRCh37
NC_000017.9:g.58919664T=	NCBI36
NG_011648.1:g.16499T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2306-77T= MANE Select	ENSP00000290866.4:n.2306-77T=
ENST00000290863.10:c.584-77T=	ENSP00000290863.6:n.584-77T=
ENST00000290866.9:c.2306-77T=	ENSP00000290866.4:n.2306-77T=
ENST00000413513.7:c.584-77T=	ENSP00000392247.3:n.584-77T=
ENST00000428043.5:c.2306-77T=	ENSP00000397593.2:n.2306-77T=
ENST00000577647.2:c.584-77T=	ENSP00000464149.1:n.584-77T=
ENST00000578839.5:c.*376-77T=	ENSP00000462110.2:n.*376-77T=
ENST00000579204.1:c.488T=	ENSP00000464629.1:n.488T=
ENST00000579314.5:c.585T=	ENSP00000462599.1:p.Ala195=
ENST00000582005.5:c.*226-77T=	ENSP00000462002.1:n.*226-77T=
ENST00000582761.1:c.74-77T=	ENSP00000462909.1:n.74-77T=
ENST00000584865.5:n.252-77T=
NM_000789.3:c.2306-77T=	NP_000780.1:n.2306-77T=
NM_001178057.1:c.584-77T=	NP_001171528.1:n.584-77T=
NM_152830.2:c.584-77T=	NP_690043.1:n.584-77T=
XM_005257110.1:c.1757-77T=	XP_005257167.1:n.1757-77T=
XM_006721737.2:c.644-77T=	XP_006721800.2:n.644-77T=
XM_006721737.3:c.644-77T=	XP_006721800.2:n.644-77T=
NM_000789.4:c.2306-77T= MANE Select	NP_000780.1:n.2306-77T=
NM_001178057.2:c.584-77T=	NP_001171528.1:n.584-77T=
NM_152830.3:c.584-77T=	NP_690043.1:n.584-77T=
NM_001382700.1:c.1739-77T=	NP_001369629.1:n.1739-77T=
NM_001382701.1:c.1454-77T=	NP_001369630.1:n.1454-77T=
NM_001382702.1:c.236-77T=	NP_001369631.1:n.236-77T=
NR_168483.1:n.607T=