Canonical Allele Identifier: CA400538180

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477099G>A , CM000679.2:g.63477099G>A	GRCh38
NC_000017.10:g.61554460G>A , CM000679.1:g.61554460G>A	GRCh37
NC_000017.9:g.58908192G>A	NCBI36
NG_011648.1:g.5027G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.5G>A MANE Select	ENSP00000290866.4:p.Gly2Glu
ENST00000290866.9:c.5G>A	ENSP00000290866.4:p.Gly2Glu
ENST00000428043.5:c.5G>A	ENSP00000397593.2:p.Gly2Glu
ENST00000579462.1:n.30G>A
ENST00000582678.5:c.5G>A	ENSP00000462995.1:p.Gly2Glu
ENST00000583336.5:n.39G>A
ENST00000584529.5:n.39G>A
NM_000789.3:c.5G>A	NP_000780.1:p.Gly2Glu
XM_005257110.1:c.-451G>A	XP_005257167.1:n.-451G>A
NM_000789.4:c.5G>A MANE Select	NP_000780.1:p.Gly2Glu
NM_001382700.1:c.-231G>A	NP_001369629.1:n.-231G>A
NM_001382701.1:c.-610G>A	NP_001369630.1:n.-610G>A