Canonical Allele Identifier: CA400567329
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63496899A>G , CM000679.2:g.63496899A>G GRCh38
NC_000017.10:g.61574260A>G , CM000679.1:g.61574260A>G GRCh37
NC_000017.9:g.58927992A>G NCBI36
NG_011648.1:g.24827A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3605A>G MANE Select ENSP00000290866.4:p.Lys1202Arg
ENST00000290863.10:c.1883A>G ENSP00000290863.6:p.Lys628Arg
ENST00000290866.9:c.3605A>G ENSP00000290866.4:p.Lys1202Arg
ENST00000413513.7:c.1760A>G ENSP00000392247.3:p.Lys587Arg
ENST00000428043.5:c.3605A>G ENSP00000397593.2:p.Lys1202Arg
ENST00000577418.5:n.615A>G
ENST00000577647.2:c.1883A>G ENSP00000464149.1:p.Lys628Arg
ENST00000578839.5:c.*1360A>G ENSP00000462110.2:n.*1360A>G
ENST00000579314.5:c.*1334A>G ENSP00000462599.1:n.*1334A>G
ENST00000579409.1:c.292A>G
ENST00000582244.1:n.479A>G
NM_000789.3:c.3605A>G NP_000780.1:p.Lys1202Arg
NM_001178057.1:c.1760A>G NP_001171528.1:p.Lys587Arg
NM_152830.2:c.1883A>G NP_690043.1:p.Lys628Arg
XM_005257110.1:c.3056A>G XP_005257167.1:p.Lys1019Arg
XM_006721737.2:c.1943A>G XP_006721800.2:p.Lys648Arg
XM_006721737.3:c.1943A>G XP_006721800.2:p.Lys648Arg
NM_000789.4:c.3605A>G MANE Select NP_000780.1:p.Lys1202Arg
NM_001178057.2:c.1760A>G NP_001171528.1:p.Lys587Arg
NM_152830.3:c.1883A>G NP_690043.1:p.Lys628Arg
NM_001382700.1:c.3038A>G NP_001369629.1:p.Lys1013Arg
NM_001382701.1:c.2753A>G NP_001369630.1:p.Lys918Arg
NM_001382702.1:c.1220A>G NP_001369631.1:p.Lys407Arg
NR_168483.1:n.1983A>G