Canonical Allele Identifier: CA2269943269

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63483697C= , CM000679.2:g.63483697C=	GRCh38
NC_000017.10:g.61561058C= , CM000679.1:g.61561058C=	GRCh37
NC_000017.9:g.58914790C=	NCBI36
NG_011648.1:g.11625C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1586+139C= MANE Select	ENSP00000290866.4:n.1586+139C=
ENST00000290866.9:c.1586+139C=	ENSP00000290866.4:n.1586+139C=
ENST00000428043.5:c.1586+139C=	ENSP00000397593.2:n.1586+139C=
ENST00000582678.5:c.*985+139C=	ENSP00000462995.1:n.*985+139C=
NM_000789.3:c.1586+139C=	NP_000780.1:n.1586+139C=
XM_005257110.1:c.1037+139C=	XP_005257167.1:n.1037+139C=
NM_000789.4:c.1586+139C= MANE Select	NP_000780.1:n.1586+139C=
NM_001382700.1:c.1019+139C=	NP_001369629.1:n.1019+139C=
NM_001382701.1:c.734+139C=	NP_001369630.1:n.734+139C=