Canonical Allele Identifier: CA501341396

Gene: ACE

Linked Data

• gnomAD v4: 17-63477268-A-G
• MyVariant Identifiers: chr17:g.61554629A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477268A>G , CM000679.2:g.63477268A>G	GRCh38
NC_000017.10:g.61554629A>G , CM000679.1:g.61554629A>G	GRCh37
NC_000017.9:g.58908361A>G	NCBI36
NG_011648.1:g.5196A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.174A>G MANE Select	ENSP00000290866.4:p.Glu58=
ENST00000290866.9:c.174A>G	ENSP00000290866.4:p.Glu58=
ENST00000428043.5:c.174A>G	ENSP00000397593.2:p.Glu58=
ENST00000579462.1:n.199A>G
ENST00000582678.5:c.174A>G	ENSP00000462995.1:p.Glu58=
ENST00000583336.5:n.208A>G
ENST00000584529.5:n.208A>G
NM_000789.3:c.174A>G	NP_000780.1:p.Glu58=
XM_005257110.1:c.-282A>G	XP_005257167.1:n.-282A>G
NM_000789.4:c.174A>G MANE Select	NP_000780.1:p.Glu58=
NM_001382700.1:c.-62A>G	NP_001369629.1:n.-62A>G
NM_001382701.1:c.-441A>G	NP_001369630.1:n.-441A>G