Canonical Allele Identifier: CA501342271

Gene: ACE

Linked Data

• gnomAD v4: 17-63497159-A-G
• MyVariant Identifiers: chr17:g.61574520A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497159A>G , CM000679.2:g.63497159A>G	GRCh38
NC_000017.10:g.61574520A>G , CM000679.1:g.61574520A>G	GRCh37
NC_000017.9:g.58928252A>G	NCBI36
NG_011648.1:g.25087A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3714A>G MANE Select	ENSP00000290866.4:p.Pro1238=
ENST00000290863.10:c.1992A>G	ENSP00000290863.6:p.Pro664=
ENST00000290866.9:c.3714A>G	ENSP00000290866.4:p.Pro1238=
ENST00000413513.7:c.1869A>G	ENSP00000392247.3:p.Pro623=
ENST00000428043.5:c.*136A>G	ENSP00000397593.2:n.*136A>G
ENST00000577418.5:n.724A>G
ENST00000577647.2:c.1969+174A>G	ENSP00000464149.1:n.1969+174A>G
ENST00000578839.5:c.*1469A>G	ENSP00000462110.2:n.*1469A>G
ENST00000579314.5:c.*1443A>G	ENSP00000462599.1:n.*1443A>G
NM_000789.3:c.3714A>G	NP_000780.1:p.Pro1238=
NM_001178057.1:c.1869A>G	NP_001171528.1:p.Pro623=
NM_152830.2:c.1992A>G	NP_690043.1:p.Pro664=
XM_005257110.1:c.3165A>G	XP_005257167.1:p.Pro1055=
XM_006721737.2:c.2052A>G	XP_006721800.2:p.Pro684=
XM_006721737.3:c.2052A>G	XP_006721800.2:p.Pro684=
NM_000789.4:c.3714A>G MANE Select	NP_000780.1:p.Pro1238=
NM_001178057.2:c.1869A>G	NP_001171528.1:p.Pro623=
NM_152830.3:c.1992A>G	NP_690043.1:p.Pro664=
NM_001382700.1:c.3147A>G	NP_001369629.1:p.Pro1049=
NM_001382701.1:c.2862A>G	NP_001369630.1:p.Pro954=
NM_001382702.1:c.1329A>G	NP_001369631.1:p.Pro443=
NR_168483.1:n.2092A>G