Canonical Allele Identifier: CA400567809
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63496969C>G , CM000679.2:g.63496969C>G GRCh38
NC_000017.10:g.61574330C>G , CM000679.1:g.61574330C>G GRCh37
NC_000017.9:g.58928062C>G NCBI36
NG_011648.1:g.24897C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3675C>G MANE Select ENSP00000290866.4:p.Asn1225Lys
ENST00000290863.10:c.1953C>G ENSP00000290863.6:p.Asn651Lys
ENST00000290866.9:c.3675C>G ENSP00000290866.4:p.Asn1225Lys
ENST00000413513.7:c.1830C>G ENSP00000392247.3:p.Asn610Lys
ENST00000428043.5:c.3675C>G ENSP00000397593.2:p.Asn1225Lys
ENST00000577418.5:n.685C>G
ENST00000577647.2:c.1953C>G ENSP00000464149.1:p.Asn651Lys
ENST00000578839.5:c.*1430C>G ENSP00000462110.2:n.*1430C>G
ENST00000579314.5:c.*1404C>G ENSP00000462599.1:n.*1404C>G
ENST00000579409.1:c.362C>G
ENST00000582244.1:n.549C>G
NM_000789.3:c.3675C>G NP_000780.1:p.Asn1225Lys
NM_001178057.1:c.1830C>G NP_001171528.1:p.Asn610Lys
NM_152830.2:c.1953C>G NP_690043.1:p.Asn651Lys
XM_005257110.1:c.3126C>G XP_005257167.1:p.Asn1042Lys
XM_006721737.2:c.2013C>G XP_006721800.2:p.Asn671Lys
XM_006721737.3:c.2013C>G XP_006721800.2:p.Asn671Lys
NM_000789.4:c.3675C>G MANE Select NP_000780.1:p.Asn1225Lys
NM_001178057.2:c.1830C>G NP_001171528.1:p.Asn610Lys
NM_152830.3:c.1953C>G NP_690043.1:p.Asn651Lys
NM_001382700.1:c.3108C>G NP_001369629.1:p.Asn1036Lys
NM_001382701.1:c.2823C>G NP_001369630.1:p.Asn941Lys
NM_001382702.1:c.1290C>G NP_001369631.1:p.Asn430Lys
NR_168483.1:n.2053C>G