Canonical Allele Identifier: CA8699034

Gene: ACE

Linked Data

• dbSNP Id: rs764488884
• ExAC: 17:61555451 C / G
• gnomAD v2: 17-61555451-C-G
• gnomAD v3: 17-63478090-C-G
• gnomAD v4: 17-63478090-C-G
• MyVariant Identifiers: chr17:g.61555451C>G (hg19) ; chr17:g.63478090C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478090C>G , CM000679.2:g.63478090C>G	GRCh38
NC_000017.10:g.61555451C>G , CM000679.1:g.61555451C>G	GRCh37
NC_000017.9:g.58909183C>G	NCBI36
NG_011648.1:g.6018C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.409C>G MANE Select	ENSP00000290866.4:p.Arg137Gly
ENST00000290866.9:c.409C>G	ENSP00000290866.4:p.Arg137Gly
ENST00000428043.5:c.409C>G	ENSP00000397593.2:p.Arg137Gly
ENST00000579462.1:n.434C>G
ENST00000580318.1:n.598C>G
ENST00000582627.1:c.409C>G	ENSP00000462280.1:p.Arg137Gly
ENST00000582678.5:c.409C>G	ENSP00000462995.1:p.Arg137Gly
ENST00000583336.5:n.443C>G
ENST00000584529.5:n.443C>G
NM_000789.3:c.409C>G	NP_000780.1:p.Arg137Gly
XM_005257110.1:c.-47C>G	XP_005257167.1:n.-47C>G
NM_000789.4:c.409C>G MANE Select	NP_000780.1:p.Arg137Gly
NM_001382700.1:c.174C>G	NP_001369629.1:p.Ser58Arg
NM_001382701.1:c.-206C>G	NP_001369630.1:n.-206C>G