Canonical Allele Identifier: CA2269939737

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477160G= , CM000679.2:g.63477160G=	GRCh38
NC_000017.10:g.61554521G= , CM000679.1:g.61554521G=	GRCh37
NC_000017.9:g.58908253G=	NCBI36
NG_011648.1:g.5088G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.66G= MANE Select	ENSP00000290866.4:p.Leu22=
ENST00000290866.9:c.66G=	ENSP00000290866.4:p.Leu22=
ENST00000428043.5:c.66G=	ENSP00000397593.2:p.Leu22=
ENST00000579462.1:n.91G=
ENST00000582678.5:c.66G=	ENSP00000462995.1:p.Leu22=
ENST00000583336.5:n.100G=
ENST00000584529.5:n.100G=
NM_000789.3:c.66G=	NP_000780.1:p.Leu22=
XM_005257110.1:c.-390G=	XP_005257167.1:n.-390G=
NM_000789.4:c.66G= MANE Select	NP_000780.1:p.Leu22=
NM_001382700.1:c.-170G=	NP_001369629.1:n.-170G=
NM_001382701.1:c.-549G=	NP_001369630.1:n.-549G=