Canonical Allele Identifier: CA2269946095

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488974T= , CM000679.2:g.63488974T=	GRCh38
NC_000017.10:g.61566335T= , CM000679.1:g.61566335T=	GRCh37
NC_000017.9:g.58920067T=	NCBI36
NG_011648.1:g.16902T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2483T= MANE Select	ENSP00000290866.4:p.Met828=
ENST00000290863.10:c.761T=	ENSP00000290863.6:p.Met254=
ENST00000290866.9:c.2483T=	ENSP00000290866.4:p.Met828=
ENST00000413513.7:c.761T=	ENSP00000392247.3:p.Met254=
ENST00000428043.5:c.2483T=	ENSP00000397593.2:p.Met828=
ENST00000577647.2:c.761T=	ENSP00000464149.1:p.Met254=
ENST00000578839.5:c.*519+183T=	ENSP00000462110.2:n.*519+183T=
ENST00000579204.1:c.742T=	ENSP00000464629.1:n.742T=
ENST00000579314.5:c.*212T=	ENSP00000462599.1:n.*212T=
ENST00000582005.5:c.*403T=	ENSP00000462002.1:n.*403T=
ENST00000582761.1:c.251T=	ENSP00000462909.1:p.Met84=
ENST00000584865.5:n.429T=
NM_000789.3:c.2483T=	NP_000780.1:p.Met828=
NM_001178057.1:c.761T=	NP_001171528.1:p.Met254=
NM_152830.2:c.761T=	NP_690043.1:p.Met254=
XM_005257110.1:c.1934T=	XP_005257167.1:p.Met645=
XM_006721737.2:c.821T=	XP_006721800.2:p.Met274=
XM_006721737.3:c.821T=	XP_006721800.2:p.Met274=
NM_000789.4:c.2483T= MANE Select	NP_000780.1:p.Met828=
NM_001178057.2:c.761T=	NP_001171528.1:p.Met254=
NM_152830.3:c.761T=	NP_690043.1:p.Met254=
NM_001382700.1:c.1916T=	NP_001369629.1:p.Met639=
NM_001382701.1:c.1631T=	NP_001369630.1:p.Met544=
NM_001382702.1:c.379+183T=	NP_001369631.1:n.379+183T=
NR_168483.1:n.861T=