Canonical Allele Identifier: CA2639243182
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63497081_63497103dup , CM000679.2:g.63497081_63497103dup GRCh38
NC_000017.10:g.61574442_61574464dup , CM000679.1:g.61574442_61574464dup GRCh37
NC_000017.9:g.58928174_58928196dup NCBI36
NG_011648.1:g.25009_25031dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3692-56_3692-34dup MANE Select ENSP00000290866.4:n.3692-56_3692-34dup
ENST00000290863.10:c.1970-56_1970-34dup ENSP00000290863.6:n.1970-56_1970-34dup
ENST00000290866.9:c.3692-56_3692-34dup ENSP00000290866.4:n.3692-56_3692-34dup
ENST00000413513.7:c.1847-56_1847-34dup ENSP00000392247.3:n.1847-56_1847-34dup
ENST00000428043.5:c.*58_*80dup ENSP00000397593.2:n.*58_*80dup
ENST00000577418.5:n.702-56_702-34dup
ENST00000577647.2:c.1969+96_1969+118dup ENSP00000464149.1:n.1969+96_1969+118dup
ENST00000578839.5:c.*1447-56_*1447-34dup ENSP00000462110.2:n.*1447-56_*1447-34dup
ENST00000579314.5:c.*1421-56_*1421-34dup ENSP00000462599.1:n.*1421-56_*1421-34dup
ENST00000579409.1:c.474_496dup
NM_000789.3:c.3692-56_3692-34dup NP_000780.1:n.3692-56_3692-34dup
NM_001178057.1:c.1847-56_1847-34dup NP_001171528.1:n.1847-56_1847-34dup
NM_152830.2:c.1970-56_1970-34dup NP_690043.1:n.1970-56_1970-34dup
XM_005257110.1:c.3143-56_3143-34dup XP_005257167.1:n.3143-56_3143-34dup
XM_006721737.2:c.2030-56_2030-34dup XP_006721800.2:n.2030-56_2030-34dup
XM_006721737.3:c.2030-56_2030-34dup XP_006721800.2:n.2030-56_2030-34dup
NM_000789.4:c.3692-56_3692-34dup MANE Select NP_000780.1:n.3692-56_3692-34dup
NM_001178057.2:c.1847-56_1847-34dup NP_001171528.1:n.1847-56_1847-34dup
NM_152830.3:c.1970-56_1970-34dup NP_690043.1:n.1970-56_1970-34dup
NM_001382700.1:c.3125-56_3125-34dup NP_001369629.1:n.3125-56_3125-34dup
NM_001382701.1:c.2840-56_2840-34dup NP_001369630.1:n.2840-56_2840-34dup
NM_001382702.1:c.1307-56_1307-34dup NP_001369631.1:n.1307-56_1307-34dup
NR_168483.1:n.2070-56_2070-34dup