Canonical Allele Identifier: CA2269949756

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496805A= , CM000679.2:g.63496805A=	GRCh38
NC_000017.10:g.61574166A= , CM000679.1:g.61574166A=	GRCh37
NC_000017.9:g.58927898A=	NCBI36
NG_011648.1:g.24733A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3511A= MANE Select	ENSP00000290866.4:p.Met1171=
ENST00000290863.10:c.1789A=	ENSP00000290863.6:p.Met597=
ENST00000290866.9:c.3511A=	ENSP00000290866.4:p.Met1171=
ENST00000413513.7:c.1666A=	ENSP00000392247.3:p.Met556=
ENST00000428043.5:c.3511A=	ENSP00000397593.2:p.Met1171=
ENST00000577418.5:n.521A=
ENST00000577647.2:c.1789A=	ENSP00000464149.1:p.Met597=
ENST00000578839.5:c.*1266A=	ENSP00000462110.2:n.*1266A=
ENST00000579314.5:c.*1240A=	ENSP00000462599.1:n.*1240A=
ENST00000579409.1:c.198A=
ENST00000582244.1:n.385A=
NM_000789.3:c.3511A=	NP_000780.1:p.Met1171=
NM_001178057.1:c.1666A=	NP_001171528.1:p.Met556=
NM_152830.2:c.1789A=	NP_690043.1:p.Met597=
XM_005257110.1:c.2962A=	XP_005257167.1:p.Met988=
XM_006721737.2:c.1849A=	XP_006721800.2:p.Met617=
XM_006721737.3:c.1849A=	XP_006721800.2:p.Met617=
NM_000789.4:c.3511A= MANE Select	NP_000780.1:p.Met1171=
NM_001178057.2:c.1666A=	NP_001171528.1:p.Met556=
NM_152830.3:c.1789A=	NP_690043.1:p.Met597=
NM_001382700.1:c.2944A=	NP_001369629.1:p.Met982=
NM_001382701.1:c.2659A=	NP_001369630.1:p.Met887=
NM_001382702.1:c.1126A=	NP_001369631.1:p.Met376=
NR_168483.1:n.1889A=