Canonical Allele Identifier: CA2639263294
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63486927_63486948dup , CM000679.2:g.63486927_63486948dup GRCh38
NC_000017.10:g.61564288_61564309dup , CM000679.1:g.61564288_61564309dup GRCh37
NC_000017.9:g.58918020_58918041dup NCBI36
NG_011648.1:g.14855_14876dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.2218-59_2218-38dup MANE Select ENSP00000290866.4:n.2218-59_2218-38dup
ENST00000290863.10:c.496-59_496-38dup ENSP00000290863.6:n.496-59_496-38dup
ENST00000290866.9:c.2218-59_2218-38dup ENSP00000290866.4:n.2218-59_2218-38dup
ENST00000413513.7:c.496-59_496-38dup ENSP00000392247.3:n.496-59_496-38dup
ENST00000428043.5:c.2218-59_2218-38dup ENSP00000397593.2:n.2218-59_2218-38dup
ENST00000577647.2:c.496-59_496-38dup ENSP00000464149.1:n.496-59_496-38dup
ENST00000578839.5:c.*288-59_*288-38dup ENSP00000462110.2:n.*288-59_*288-38dup
ENST00000579204.1:c.399-59_399-38dup ENSP00000464629.1:n.399-59_399-38dup
ENST00000579314.5:c.496-59_496-38dup ENSP00000462599.1:n.496-59_496-38dup
ENST00000579726.5:c.780-59_780-38dup
ENST00000582005.5:c.*138-59_*138-38dup ENSP00000462002.1:n.*138-59_*138-38dup
ENST00000584865.5:n.105_126dup
NM_000789.3:c.2218-59_2218-38dup NP_000780.1:n.2218-59_2218-38dup
NM_001178057.1:c.496-59_496-38dup NP_001171528.1:n.496-59_496-38dup
NM_152830.2:c.496-59_496-38dup NP_690043.1:n.496-59_496-38dup
XM_005257110.1:c.1669-59_1669-38dup XP_005257167.1:n.1669-59_1669-38dup
XM_006721737.2:c.556-59_556-38dup XP_006721800.2:n.556-59_556-38dup
XM_006721737.3:c.556-59_556-38dup XP_006721800.2:n.556-59_556-38dup
NM_000789.4:c.2218-59_2218-38dup MANE Select NP_000780.1:n.2218-59_2218-38dup
NM_001178057.2:c.496-59_496-38dup NP_001171528.1:n.496-59_496-38dup
NM_152830.3:c.496-59_496-38dup NP_690043.1:n.496-59_496-38dup
NM_001382700.1:c.1651-59_1651-38dup NP_001369629.1:n.1651-59_1651-38dup
NM_001382701.1:c.1366-59_1366-38dup NP_001369630.1:n.1366-59_1366-38dup
NM_001382702.1:c.148-59_148-38dup NP_001369631.1:n.148-59_148-38dup
NR_168483.1:n.518-59_518-38dup