Canonical Allele Identifier: CA773972286
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1164240705

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63495079_63495080insA , CM000679.2:g.63495079_63495080insA GRCh38
NC_000017.10:g.61572440_61572441insA , CM000679.1:g.61572440_61572441insA GRCh37
NC_000017.9:g.58926172_58926173insA NCBI36
NG_011648.1:g.23007_23008insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3380+609_3380+610insA MANE Select ENSP00000290866.4:n.3380+609_3380+610insA
ENST00000290863.10:c.1658+609_1658+610insA ENSP00000290863.6:n.1658+609_1658+610insA
ENST00000290866.9:c.3380+609_3380+610insA ENSP00000290866.4:n.3380+609_3380+610insA
ENST00000413513.7:c.1658+609_1658+610insA ENSP00000392247.3:n.1658+609_1658+610insA
ENST00000428043.5:c.3380+609_3380+610insA ENSP00000397593.2:n.3380+609_3380+610insA
ENST00000577418.5:n.390+609_390+610insA
ENST00000577647.2:c.1658+609_1658+610insA ENSP00000464149.1:n.1658+609_1658+610insA
ENST00000578839.5:c.*1258+609_*1258+610insA ENSP00000462110.2:n.*1258+609_*1258+610insA
ENST00000579314.5:c.*1109+609_*1109+610insA ENSP00000462599.1:n.*1109+609_*1109+610insA
ENST00000579409.1:c.67+609_67+610insA
NM_000789.3:c.3380+609_3380+610insA NP_000780.1:n.3380+609_3380+610insA
NM_001178057.1:c.1658+609_1658+610insA NP_001171528.1:n.1658+609_1658+610insA
NM_152830.2:c.1658+609_1658+610insA NP_690043.1:n.1658+609_1658+610insA
XM_005257110.1:c.2831+609_2831+610insA XP_005257167.1:n.2831+609_2831+610insA
XM_006721737.2:c.1718+609_1718+610insA XP_006721800.2:n.1718+609_1718+610insA
XM_006721737.3:c.1718+609_1718+610insA XP_006721800.2:n.1718+609_1718+610insA
NM_000789.4:c.3380+609_3380+610insA MANE Select NP_000780.1:n.3380+609_3380+610insA
NM_001178057.2:c.1658+609_1658+610insA NP_001171528.1:n.1658+609_1658+610insA
NM_152830.3:c.1658+609_1658+610insA NP_690043.1:n.1658+609_1658+610insA
NM_001382700.1:c.2813+609_2813+610insA NP_001369629.1:n.2813+609_2813+610insA
NM_001382701.1:c.2528+609_2528+610insA NP_001369630.1:n.2528+609_2528+610insA
NM_001382702.1:c.1118+609_1118+610insA NP_001369631.1:n.1118+609_1118+610insA
NR_168483.1:n.1758+609_1758+610insA