Canonical Allele Identifier: CA2639263348
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63487082_63487083insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC , CM000679.2:g.63487082_63487083insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC GRCh38
NC_000017.10:g.61564443_61564444insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC , CM000679.1:g.61564443_61564444insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC GRCh37
NC_000017.9:g.58918175_58918176insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC NCBI36
NG_011648.1:g.15010_15011insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC MANE Select ENSP00000290866.4:n.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGA...
ENST00000290863.10:c.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000290863.6:n.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGA...
ENST00000290866.9:c.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000290866.4:n.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGA...
ENST00000413513.7:c.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000392247.3:n.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGA...
ENST00000428043.5:c.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000397593.2:n.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGA...
ENST00000577647.2:c.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000464149.1:n.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGA...
ENST00000578839.5:c.*375+9_*375+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000462110.2:n.*375+9_*375+10insGAGTGAGAGAGGTGAGAGAGGTGA...
ENST00000579204.1:c.486+9_486+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000464629.1:n.486+9_486+10insGAGTGAGAGAGGTGAGAGAGGTGAGA...
ENST00000579314.5:c.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000462599.1:n.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGA...
ENST00000582005.5:c.*225+9_*225+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000462002.1:n.*225+9_*225+10insGAGTGAGAGAGGTGAGAGAGGTGA...
ENST00000582761.1:c.73+9_73+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC ENSP00000462909.1:n.73+9_73+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGC...
ENST00000584865.5:n.251+9_251+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC
NM_000789.3:c.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC NP_000780.1:n.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCA...
NM_001178057.1:c.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC NP_001171528.1:n.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCC...
NM_152830.2:c.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC NP_690043.1:n.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGG...
XM_005257110.1:c.1756+9_1756+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC XP_005257167.1:n.1756+9_1756+10insGAGTGAGAGAGGTGAGAGAGGTGAGAG...
XM_006721737.2:c.643+9_643+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC XP_006721800.2:n.643+9_643+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCC...
XM_006721737.3:c.643+9_643+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC XP_006721800.2:n.643+9_643+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCC...
NM_000789.4:c.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC MANE Select NP_000780.1:n.2305+9_2305+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCA...
NM_001178057.2:c.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC NP_001171528.1:n.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCC...
NM_152830.3:c.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC NP_690043.1:n.583+9_583+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGG...
NM_001382700.1:c.1738+9_1738+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC NP_001369629.1:n.1738+9_1738+10insGAGTGAGAGAGGTGAGAGAGGTGAGAG...
NM_001382701.1:c.1453+9_1453+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC NP_001369630.1:n.1453+9_1453+10insGAGTGAGAGAGGTGAGAGAGGTGAGAG...
NM_001382702.1:c.235+9_235+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC NP_001369631.1:n.235+9_235+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCC...
NR_168483.1:n.605+9_605+10insGAGTGAGAGAGGTGAGAGAGGTGAGAGCCAGGTGAGAGC