Canonical Allele Identifier: CA2269946102

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488989C= , CM000679.2:g.63488989C=	GRCh38
NC_000017.10:g.61566350C= , CM000679.1:g.61566350C=	GRCh37
NC_000017.9:g.58920082C=	NCBI36
NG_011648.1:g.16917C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2498C= MANE Select	ENSP00000290866.4:p.Ser833=
ENST00000290863.10:c.776C=	ENSP00000290863.6:p.Ser259=
ENST00000290866.9:c.2498C=	ENSP00000290866.4:p.Ser833=
ENST00000413513.7:c.776C=	ENSP00000392247.3:p.Ser259=
ENST00000428043.5:c.2498C=	ENSP00000397593.2:p.Ser833=
ENST00000577647.2:c.776C=	ENSP00000464149.1:p.Ser259=
ENST00000578839.5:c.*519+198C=	ENSP00000462110.2:n.*519+198C=
ENST00000579204.1:c.757C=	ENSP00000464629.1:n.757C=
ENST00000579314.5:c.*227C=	ENSP00000462599.1:n.*227C=
ENST00000582005.5:c.*418C=	ENSP00000462002.1:n.*418C=
ENST00000582761.1:c.266C=	ENSP00000462909.1:p.Ser89=
ENST00000584865.5:n.444C=
NM_000789.3:c.2498C=	NP_000780.1:p.Ser833=
NM_001178057.1:c.776C=	NP_001171528.1:p.Ser259=
NM_152830.2:c.776C=	NP_690043.1:p.Ser259=
XM_005257110.1:c.1949C=	XP_005257167.1:p.Ser650=
XM_006721737.2:c.836C=	XP_006721800.2:p.Ser279=
XM_006721737.3:c.836C=	XP_006721800.2:p.Ser279=
NM_000789.4:c.2498C= MANE Select	NP_000780.1:p.Ser833=
NM_001178057.2:c.776C=	NP_001171528.1:p.Ser259=
NM_152830.3:c.776C=	NP_690043.1:p.Ser259=
NM_001382700.1:c.1931C=	NP_001369629.1:p.Ser644=
NM_001382701.1:c.1646C=	NP_001369630.1:p.Ser549=
NM_001382702.1:c.379+198C=	NP_001369631.1:n.379+198C=
NR_168483.1:n.876C=