Canonical Allele Identifier: CA2639263284
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63486915_63486916insCACTGCCCCCAGGCCCCATGGGCTG , CM000679.2:g.63486915_63486916insCACTGCCCCCAGGCCCCATGGGCTG GRCh38
NC_000017.10:g.61564276_61564277insCACTGCCCCCAGGCCCCATGGGCTG , CM000679.1:g.61564276_61564277insCACTGCCCCCAGGCCCCATGGGCTG GRCh37
NC_000017.9:g.58918008_58918009insCACTGCCCCCAGGCCCCATGGGCTG NCBI36
NG_011648.1:g.14843_14844insCACTGCCCCCAGGCCCCATGGGCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGCTG MANE Select ENSP00000290866.4:n.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGC...
ENST00000290863.10:c.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG ENSP00000290863.6:n.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG...
ENST00000290866.9:c.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGCTG ENSP00000290866.4:n.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGC...
ENST00000413513.7:c.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG ENSP00000392247.3:n.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG...
ENST00000428043.5:c.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGCTG ENSP00000397593.2:n.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGC...
ENST00000577647.2:c.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG ENSP00000464149.1:n.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG...
ENST00000578839.5:c.*288-71_*288-70insCACTGCCCCCAGGCCCCATGGGCTG ENSP00000462110.2:n.*288-71_*288-70insCACTGCCCCCAGGCCCCATGGGC...
ENST00000579204.1:c.399-71_399-70insCACTGCCCCCAGGCCCCATGGGCTG ENSP00000464629.1:n.399-71_399-70insCACTGCCCCCAGGCCCCATGGGCTG...
ENST00000579314.5:c.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG ENSP00000462599.1:n.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG...
ENST00000579726.5:c.780-71_780-70insCACTGCCCCCAGGCCCCATGGGCTG
ENST00000582005.5:c.*138-71_*138-70insCACTGCCCCCAGGCCCCATGGGCTG ENSP00000462002.1:n.*138-71_*138-70insCACTGCCCCCAGGCCCCATGGGC...
ENST00000584865.5:n.93_94insCACTGCCCCCAGGCCCCATGGGCTG
NM_000789.3:c.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGCTG NP_000780.1:n.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGCTG
NM_001178057.1:c.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG NP_001171528.1:n.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG
NM_152830.2:c.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG NP_690043.1:n.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG
XM_005257110.1:c.1669-71_1669-70insCACTGCCCCCAGGCCCCATGGGCTG XP_005257167.1:n.1669-71_1669-70insCACTGCCCCCAGGCCCCATGGGCTG
XM_006721737.2:c.556-71_556-70insCACTGCCCCCAGGCCCCATGGGCTG XP_006721800.2:n.556-71_556-70insCACTGCCCCCAGGCCCCATGGGCTG
XM_006721737.3:c.556-71_556-70insCACTGCCCCCAGGCCCCATGGGCTG XP_006721800.2:n.556-71_556-70insCACTGCCCCCAGGCCCCATGGGCTG
NM_000789.4:c.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGCTG MANE Select NP_000780.1:n.2218-71_2218-70insCACTGCCCCCAGGCCCCATGGGCTG
NM_001178057.2:c.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG NP_001171528.1:n.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG
NM_152830.3:c.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG NP_690043.1:n.496-71_496-70insCACTGCCCCCAGGCCCCATGGGCTG
NM_001382700.1:c.1651-71_1651-70insCACTGCCCCCAGGCCCCATGGGCTG NP_001369629.1:n.1651-71_1651-70insCACTGCCCCCAGGCCCCATGGGCTG
NM_001382701.1:c.1366-71_1366-70insCACTGCCCCCAGGCCCCATGGGCTG NP_001369630.1:n.1366-71_1366-70insCACTGCCCCCAGGCCCCATGGGCTG
NM_001382702.1:c.148-71_148-70insCACTGCCCCCAGGCCCCATGGGCTG NP_001369631.1:n.148-71_148-70insCACTGCCCCCAGGCCCCATGGGCTG
NR_168483.1:n.518-71_518-70insCACTGCCCCCAGGCCCCATGGGCTG