Canonical Allele Identifier: CA400567906
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63496981C>A , CM000679.2:g.63496981C>A GRCh38
NC_000017.10:g.61574342C>A , CM000679.1:g.61574342C>A GRCh37
NC_000017.9:g.58928074C>A NCBI36
NG_011648.1:g.24909C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.3687C>A MANE Select ENSP00000290866.4:p.Asn1229Lys
ENST00000290863.10:c.1965C>A ENSP00000290863.6:p.Asn655Lys
ENST00000290866.9:c.3687C>A ENSP00000290866.4:p.Asn1229Lys
ENST00000413513.7:c.1842C>A ENSP00000392247.3:p.Asn614Lys
ENST00000428043.5:c.3687C>A ENSP00000397593.2:p.Asn1229Lys
ENST00000577418.5:n.697C>A
ENST00000577647.2:c.1965C>A ENSP00000464149.1:p.Asn655Lys
ENST00000578839.5:c.*1442C>A ENSP00000462110.2:n.*1442C>A
ENST00000579314.5:c.*1416C>A ENSP00000462599.1:n.*1416C>A
ENST00000579409.1:c.374C>A
ENST00000582244.1:n.561C>A
NM_000789.3:c.3687C>A NP_000780.1:p.Asn1229Lys
NM_001178057.1:c.1842C>A NP_001171528.1:p.Asn614Lys
NM_152830.2:c.1965C>A NP_690043.1:p.Asn655Lys
XM_005257110.1:c.3138C>A XP_005257167.1:p.Asn1046Lys
XM_006721737.2:c.2025C>A XP_006721800.2:p.Asn675Lys
XM_006721737.3:c.2025C>A XP_006721800.2:p.Asn675Lys
NM_000789.4:c.3687C>A MANE Select NP_000780.1:p.Asn1229Lys
NM_001178057.2:c.1842C>A NP_001171528.1:p.Asn614Lys
NM_152830.3:c.1965C>A NP_690043.1:p.Asn655Lys
NM_001382700.1:c.3120C>A NP_001369629.1:p.Asn1040Lys
NM_001382701.1:c.2835C>A NP_001369630.1:p.Asn945Lys
NM_001382702.1:c.1302C>A NP_001369631.1:p.Asn434Lys
NR_168483.1:n.2065C>A