Canonical Allele Identifier: CA2269949814

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496930C= , CM000679.2:g.63496930C=	GRCh38
NC_000017.10:g.61574291C= , CM000679.1:g.61574291C=	GRCh37
NC_000017.9:g.58928023C=	NCBI36
NG_011648.1:g.24858C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3636C= MANE Select	ENSP00000290866.4:p.Asn1212=
ENST00000290863.10:c.1914C=	ENSP00000290863.6:p.Asn638=
ENST00000290866.9:c.3636C=	ENSP00000290866.4:p.Asn1212=
ENST00000413513.7:c.1791C=	ENSP00000392247.3:p.Asn597=
ENST00000428043.5:c.3636C=	ENSP00000397593.2:p.Asn1212=
ENST00000577418.5:n.646C=
ENST00000577647.2:c.1914C=	ENSP00000464149.1:p.Asn638=
ENST00000578839.5:c.*1391C=	ENSP00000462110.2:n.*1391C=
ENST00000579314.5:c.*1365C=	ENSP00000462599.1:n.*1365C=
ENST00000579409.1:c.323C=
ENST00000582244.1:n.510C=
NM_000789.3:c.3636C=	NP_000780.1:p.Asn1212=
NM_001178057.1:c.1791C=	NP_001171528.1:p.Asn597=
NM_152830.2:c.1914C=	NP_690043.1:p.Asn638=
XM_005257110.1:c.3087C=	XP_005257167.1:p.Asn1029=
XM_006721737.2:c.1974C=	XP_006721800.2:p.Asn658=
XM_006721737.3:c.1974C=	XP_006721800.2:p.Asn658=
NM_000789.4:c.3636C= MANE Select	NP_000780.1:p.Asn1212=
NM_001178057.2:c.1791C=	NP_001171528.1:p.Asn597=
NM_152830.3:c.1914C=	NP_690043.1:p.Asn638=
NM_001382700.1:c.3069C=	NP_001369629.1:p.Asn1023=
NM_001382701.1:c.2784C=	NP_001369630.1:p.Asn928=
NM_001382702.1:c.1251C=	NP_001369631.1:p.Asn417=
NR_168483.1:n.2014C=