Canonical Allele Identifier: CA501186775
Gene: ACE HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.61566034C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488673C>A , CM000679.2:g.63488673C>A GRCh38
NC_000017.10:g.61566034C>A , CM000679.1:g.61566034C>A GRCh37
NC_000017.9:g.58919766C>A NCBI36
NG_011648.1:g.16601C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2331C>A MANE Select ENSP00000290866.4:p.Ser777=
ENST00000290863.10:c.609C>A ENSP00000290863.6:p.Ser203=
ENST00000290866.9:c.2331C>A ENSP00000290866.4:p.Ser777=
ENST00000413513.7:c.609C>A ENSP00000392247.3:p.Ser203=
ENST00000428043.5:c.2331C>A ENSP00000397593.2:p.Ser777=
ENST00000577647.2:c.609C>A ENSP00000464149.1:p.Ser203=
ENST00000578839.5:c.*401C>A ENSP00000462110.2:n.*401C>A
ENST00000579204.1:c.590C>A ENSP00000464629.1:n.590C>A
ENST00000579314.5:c.*60C>A ENSP00000462599.1:n.*60C>A
ENST00000582005.5:c.*251C>A ENSP00000462002.1:n.*251C>A
ENST00000582761.1:c.99C>A ENSP00000462909.1:p.Ser33=
ENST00000584865.5:n.277C>A
NM_000789.3:c.2331C>A NP_000780.1:p.Ser777=
NM_001178057.1:c.609C>A NP_001171528.1:p.Ser203=
NM_152830.2:c.609C>A NP_690043.1:p.Ser203=
XM_005257110.1:c.1782C>A XP_005257167.1:p.Ser594=
XM_006721737.2:c.669C>A XP_006721800.2:p.Ser223=
XM_006721737.3:c.669C>A XP_006721800.2:p.Ser223=
NM_000789.4:c.2331C>A MANE Select NP_000780.1:p.Ser777=
NM_001178057.2:c.609C>A NP_001171528.1:p.Ser203=
NM_152830.3:c.609C>A NP_690043.1:p.Ser203=
NM_001382700.1:c.1764C>A NP_001369629.1:p.Ser588=
NM_001382701.1:c.1479C>A NP_001369630.1:p.Ser493=
NM_001382702.1:c.261C>A NP_001369631.1:p.Ser87=
NR_168483.1:n.709C>A