Canonical Allele Identifier: CA2269949792

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496883A= , CM000679.2:g.63496883A=	GRCh38
NC_000017.10:g.61574244A= , CM000679.1:g.61574244A=	GRCh37
NC_000017.9:g.58927976A=	NCBI36
NG_011648.1:g.24811A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.3589A= MANE Select	ENSP00000290866.4:p.Met1197=
ENST00000290863.10:c.1867A=	ENSP00000290863.6:p.Met623=
ENST00000290866.9:c.3589A=	ENSP00000290866.4:p.Met1197=
ENST00000413513.7:c.1744A=	ENSP00000392247.3:p.Met582=
ENST00000428043.5:c.3589A=	ENSP00000397593.2:p.Met1197=
ENST00000577418.5:n.599A=
ENST00000577647.2:c.1867A=	ENSP00000464149.1:p.Met623=
ENST00000578839.5:c.*1344A=	ENSP00000462110.2:n.*1344A=
ENST00000579314.5:c.*1318A=	ENSP00000462599.1:n.*1318A=
ENST00000579409.1:c.276A=
ENST00000582244.1:n.463A=
NM_000789.3:c.3589A=	NP_000780.1:p.Met1197=
NM_001178057.1:c.1744A=	NP_001171528.1:p.Met582=
NM_152830.2:c.1867A=	NP_690043.1:p.Met623=
XM_005257110.1:c.3040A=	XP_005257167.1:p.Met1014=
XM_006721737.2:c.1927A=	XP_006721800.2:p.Met643=
XM_006721737.3:c.1927A=	XP_006721800.2:p.Met643=
NM_000789.4:c.3589A= MANE Select	NP_000780.1:p.Met1197=
NM_001178057.2:c.1744A=	NP_001171528.1:p.Met582=
NM_152830.3:c.1867A=	NP_690043.1:p.Met623=
NM_001382700.1:c.3022A=	NP_001369629.1:p.Met1008=
NM_001382701.1:c.2737A=	NP_001369630.1:p.Met913=
NM_001382702.1:c.1204A=	NP_001369631.1:p.Met402=
NR_168483.1:n.1967A=