Canonical Allele Identifier: CA292881492

Gene: ACE

Linked Data

• dbSNP Id: rs1024570279
• gnomAD v4: 17-63486637-G-A
• MyVariant Identifiers: chr17:g.61563998G>A (hg19) ; chr17:g.63486637G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486637G>A , CM000679.2:g.63486637G>A	GRCh38
NC_000017.10:g.61563998G>A , CM000679.1:g.61563998G>A	GRCh37
NC_000017.9:g.58917730G>A	NCBI36
NG_011648.1:g.14565G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2139G>A MANE Select	ENSP00000290866.4:p.Gln713=
ENST00000290863.10:c.417G>A	ENSP00000290863.6:p.Gln139=
ENST00000290866.9:c.2139G>A	ENSP00000290866.4:p.Gln713=
ENST00000413513.7:c.417G>A	ENSP00000392247.3:p.Gln139=
ENST00000428043.5:c.2139G>A	ENSP00000397593.2:p.Gln713=
ENST00000577647.2:c.417G>A	ENSP00000464149.1:p.Gln139=
ENST00000578839.5:c.*209G>A	ENSP00000462110.2:n.*209G>A
ENST00000579204.1:c.320G>A	ENSP00000464629.1:n.320G>A
ENST00000579314.5:c.417G>A	ENSP00000462599.1:p.Gln139=
ENST00000579726.5:c.701G>A
ENST00000582005.5:c.*59G>A	ENSP00000462002.1:n.*59G>A
NM_000789.3:c.2139G>A	NP_000780.1:p.Gln713=
NM_001178057.1:c.417G>A	NP_001171528.1:p.Gln139=
NM_152830.2:c.417G>A	NP_690043.1:p.Gln139=
XM_005257110.1:c.1590G>A	XP_005257167.1:p.Gln530=
XM_006721737.2:c.477G>A	XP_006721800.2:p.Gln159=
XM_006721737.3:c.477G>A	XP_006721800.2:p.Gln159=
NM_000789.4:c.2139G>A MANE Select	NP_000780.1:p.Gln713=
NM_001178057.2:c.417G>A	NP_001171528.1:p.Gln139=
NM_152830.3:c.417G>A	NP_690043.1:p.Gln139=
NM_001382700.1:c.1572G>A	NP_001369629.1:p.Gln524=
NM_001382701.1:c.1287G>A	NP_001369630.1:p.Gln429=
NM_001382702.1:c.69G>A	NP_001369631.1:p.Gln23=
NR_168483.1:n.439G>A