Canonical Allele Identifier: CA2269946109

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63489005G= , CM000679.2:g.63489005G=	GRCh38
NC_000017.10:g.61566366G= , CM000679.1:g.61566366G=	GRCh37
NC_000017.9:g.58920098G=	NCBI36
NG_011648.1:g.16933G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2514G= MANE Select	ENSP00000290866.4:p.Leu838=
ENST00000290863.10:c.792G=	ENSP00000290863.6:p.Leu264=
ENST00000290866.9:c.2514G=	ENSP00000290866.4:p.Leu838=
ENST00000413513.7:c.792G=	ENSP00000392247.3:p.Leu264=
ENST00000428043.5:c.2514G=	ENSP00000397593.2:p.Leu838=
ENST00000577647.2:c.792G=	ENSP00000464149.1:p.Leu264=
ENST00000578839.5:c.*519+214G=	ENSP00000462110.2:n.*519+214G=
ENST00000579204.1:c.773G=	ENSP00000464629.1:n.773G=
ENST00000579314.5:c.*243G=	ENSP00000462599.1:n.*243G=
ENST00000582005.5:c.*434G=	ENSP00000462002.1:n.*434G=
ENST00000582761.1:c.282G=	ENSP00000462909.1:p.Leu94=
ENST00000584865.5:n.460G=
NM_000789.3:c.2514G=	NP_000780.1:p.Leu838=
NM_001178057.1:c.792G=	NP_001171528.1:p.Leu264=
NM_152830.2:c.792G=	NP_690043.1:p.Leu264=
XM_005257110.1:c.1965G=	XP_005257167.1:p.Leu655=
XM_006721737.2:c.852G=	XP_006721800.2:p.Leu284=
XM_006721737.3:c.852G=	XP_006721800.2:p.Leu284=
NM_000789.4:c.2514G= MANE Select	NP_000780.1:p.Leu838=
NM_001178057.2:c.792G=	NP_001171528.1:p.Leu264=
NM_152830.3:c.792G=	NP_690043.1:p.Leu264=
NM_001382700.1:c.1947G=	NP_001369629.1:p.Leu649=
NM_001382701.1:c.1662G=	NP_001369630.1:p.Leu554=
NM_001382702.1:c.379+214G=	NP_001369631.1:n.379+214G=
NR_168483.1:n.892G=