Canonical Allele Identifier: CA2269945056

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486993A= , CM000679.2:g.63486993A=	GRCh38
NC_000017.10:g.61564354A= , CM000679.1:g.61564354A=	GRCh37
NC_000017.9:g.58918086A=	NCBI36
NG_011648.1:g.14921A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2225A= MANE Select	ENSP00000290866.4:p.Lys742=
ENST00000290863.10:c.503A=	ENSP00000290863.6:p.Lys168=
ENST00000290866.9:c.2225A=	ENSP00000290866.4:p.Lys742=
ENST00000413513.7:c.503A=	ENSP00000392247.3:p.Lys168=
ENST00000428043.5:c.2225A=	ENSP00000397593.2:p.Lys742=
ENST00000577647.2:c.503A=	ENSP00000464149.1:p.Lys168=
ENST00000578839.5:c.*295A=	ENSP00000462110.2:n.*295A=
ENST00000579204.1:c.406A=	ENSP00000464629.1:n.406A=
ENST00000579314.5:c.503A=	ENSP00000462599.1:p.Lys168=
ENST00000579726.5:c.787A=
ENST00000582005.5:c.*145A=	ENSP00000462002.1:n.*145A=
ENST00000584865.5:n.171A=
NM_000789.3:c.2225A=	NP_000780.1:p.Lys742=
NM_001178057.1:c.503A=	NP_001171528.1:p.Lys168=
NM_152830.2:c.503A=	NP_690043.1:p.Lys168=
XM_005257110.1:c.1676A=	XP_005257167.1:p.Lys559=
XM_006721737.2:c.563A=	XP_006721800.2:p.Lys188=
XM_006721737.3:c.563A=	XP_006721800.2:p.Lys188=
NM_000789.4:c.2225A= MANE Select	NP_000780.1:p.Lys742=
NM_001178057.2:c.503A=	NP_001171528.1:p.Lys168=
NM_152830.3:c.503A=	NP_690043.1:p.Lys168=
NM_001382700.1:c.1658A=	NP_001369629.1:p.Lys553=
NM_001382701.1:c.1373A=	NP_001369630.1:p.Lys458=
NM_001382702.1:c.155A=	NP_001369631.1:p.Lys52=
NR_168483.1:n.525A=