Canonical Allele Identifier: CA2269945029

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486945T= , CM000679.2:g.63486945T=	GRCh38
NC_000017.10:g.61564306T= , CM000679.1:g.61564306T=	GRCh37
NC_000017.9:g.58918038T=	NCBI36
NG_011648.1:g.14873T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2218-41T= MANE Select	ENSP00000290866.4:n.2218-41T=
ENST00000290863.10:c.496-41T=	ENSP00000290863.6:n.496-41T=
ENST00000290866.9:c.2218-41T=	ENSP00000290866.4:n.2218-41T=
ENST00000413513.7:c.496-41T=	ENSP00000392247.3:n.496-41T=
ENST00000428043.5:c.2218-41T=	ENSP00000397593.2:n.2218-41T=
ENST00000577647.2:c.496-41T=	ENSP00000464149.1:n.496-41T=
ENST00000578839.5:c.*288-41T=	ENSP00000462110.2:n.*288-41T=
ENST00000579204.1:c.399-41T=	ENSP00000464629.1:n.399-41T=
ENST00000579314.5:c.496-41T=	ENSP00000462599.1:n.496-41T=
ENST00000579726.5:c.780-41T=
ENST00000582005.5:c.*138-41T=	ENSP00000462002.1:n.*138-41T=
ENST00000584865.5:n.123T=
NM_000789.3:c.2218-41T=	NP_000780.1:n.2218-41T=
NM_001178057.1:c.496-41T=	NP_001171528.1:n.496-41T=
NM_152830.2:c.496-41T=	NP_690043.1:n.496-41T=
XM_005257110.1:c.1669-41T=	XP_005257167.1:n.1669-41T=
XM_006721737.2:c.556-41T=	XP_006721800.2:n.556-41T=
XM_006721737.3:c.556-41T=	XP_006721800.2:n.556-41T=
NM_000789.4:c.2218-41T= MANE Select	NP_000780.1:n.2218-41T=
NM_001178057.2:c.496-41T=	NP_001171528.1:n.496-41T=
NM_152830.3:c.496-41T=	NP_690043.1:n.496-41T=
NM_001382700.1:c.1651-41T=	NP_001369629.1:n.1651-41T=
NM_001382701.1:c.1366-41T=	NP_001369630.1:n.1366-41T=
NM_001382702.1:c.148-41T=	NP_001369631.1:n.148-41T=
NR_168483.1:n.518-41T=