Canonical Allele Identifier: CA8699730

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63484535G>A , CM000679.2:g.63484535G>A	GRCh38
NC_000017.10:g.61561896G>A , CM000679.1:g.61561896G>A	GRCh37
NC_000017.9:g.58915628G>A	NCBI36
NG_011648.1:g.12463G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000789.4:c.1915G>A MANE Select	NP_000780.1:p.Gly639Ser
ENST00000290866.10:c.1915G>A MANE Select	ENSP00000290866.4:p.Gly639Ser
NM_000789.3:c.1915G>A	NP_000780.1:p.Gly639Ser
NM_001382700.1:c.1348G>A	NP_001369629.1:p.Gly450Ser
NM_001382701.1:c.1063G>A	NP_001369630.1:p.Gly355Ser
ENST00000290866.9:c.1915G>A	ENSP00000290866.4:p.Gly639Ser
ENST00000428043.5:c.1915G>A	ENSP00000397593.2:p.Gly639Ser
ENST00000579726.5:c.198G>A
ENST00000582678.5:c.*1314G>A	ENSP00000462995.1:n.*1314G>A
XM_005257110.1:c.1366G>A	XP_005257167.1:p.Gly456Ser