Canonical Allele Identifier: CA2269946100

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488985C= , CM000679.2:g.63488985C=	GRCh38
NC_000017.10:g.61566346C= , CM000679.1:g.61566346C=	GRCh37
NC_000017.9:g.58920078C=	NCBI36
NG_011648.1:g.16913C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2494C= MANE Select	ENSP00000290866.4:p.Pro832=
ENST00000290863.10:c.772C=	ENSP00000290863.6:p.Pro258=
ENST00000290866.9:c.2494C=	ENSP00000290866.4:p.Pro832=
ENST00000413513.7:c.772C=	ENSP00000392247.3:p.Pro258=
ENST00000428043.5:c.2494C=	ENSP00000397593.2:p.Pro832=
ENST00000577647.2:c.772C=	ENSP00000464149.1:p.Pro258=
ENST00000578839.5:c.*519+194C=	ENSP00000462110.2:n.*519+194C=
ENST00000579204.1:c.753C=	ENSP00000464629.1:n.753C=
ENST00000579314.5:c.*223C=	ENSP00000462599.1:n.*223C=
ENST00000582005.5:c.*414C=	ENSP00000462002.1:n.*414C=
ENST00000582761.1:c.262C=	ENSP00000462909.1:p.Pro88=
ENST00000584865.5:n.440C=
NM_000789.3:c.2494C=	NP_000780.1:p.Pro832=
NM_001178057.1:c.772C=	NP_001171528.1:p.Pro258=
NM_152830.2:c.772C=	NP_690043.1:p.Pro258=
XM_005257110.1:c.1945C=	XP_005257167.1:p.Pro649=
XM_006721737.2:c.832C=	XP_006721800.2:p.Pro278=
XM_006721737.3:c.832C=	XP_006721800.2:p.Pro278=
NM_000789.4:c.2494C= MANE Select	NP_000780.1:p.Pro832=
NM_001178057.2:c.772C=	NP_001171528.1:p.Pro258=
NM_152830.3:c.772C=	NP_690043.1:p.Pro258=
NM_001382700.1:c.1927C=	NP_001369629.1:p.Pro643=
NM_001382701.1:c.1642C=	NP_001369630.1:p.Pro548=
NM_001382702.1:c.379+194C=	NP_001369631.1:n.379+194C=
NR_168483.1:n.872C=