Canonical Allele Identifier: CA627148161
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1555670380

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488552_63488553insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG , CM000679.2:g.63488552_63488553insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG GRCh38
NC_000017.10:g.61565913_61565914insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG , CM000679.1:g.61565913_61565914insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG GRCh37
NC_000017.9:g.58919645_58919646insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG NCBI36
NG_011648.1:g.16480_16481insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG MANE Select ENSP00000290866.4:n.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTG...
ENST00000290863.10:c.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000290863.6:n.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTC...
ENST00000290866.9:c.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000290866.4:n.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTG...
ENST00000413513.7:c.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000392247.3:n.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTC...
ENST00000428043.5:c.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000397593.2:n.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTG...
ENST00000577647.2:c.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000464149.1:n.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTC...
ENST00000578839.5:c.*376-96_*376-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000462110.2:n.*376-96_*376-95insTTTTGAGACGGAGTCTCGCTCTG...
ENST00000579204.1:c.487-18_487-17insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000464629.1:n.487-18_487-17insTTTTGAGACGGAGTCTCGCTCTGTC...
ENST00000579314.5:c.584-18_584-17insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000462599.1:n.584-18_584-17insTTTTGAGACGGAGTCTCGCTCTGTC...
ENST00000582005.5:c.*226-96_*226-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000462002.1:n.*226-96_*226-95insTTTTGAGACGGAGTCTCGCTCTG...
ENST00000582761.1:c.74-96_74-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG ENSP00000462909.1:n.74-96_74-95insTTTTGAGACGGAGTCTCGCTCTGTCGC...
ENST00000584865.5:n.252-96_252-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG
NM_000789.3:c.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG NP_000780.1:n.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCC...
NM_001178057.1:c.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG NP_001171528.1:n.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCC...
NM_152830.2:c.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG NP_690043.1:n.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAG...
XM_005257110.1:c.1757-96_1757-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG XP_005257167.1:n.1757-96_1757-95insTTTTGAGACGGAGTCTCGCTCTGTCG...
XM_006721737.2:c.644-96_644-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG XP_006721800.2:n.644-96_644-95insTTTTGAGACGGAGTCTCGCTCTGTCGCC...
XM_006721737.3:c.644-96_644-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG XP_006721800.2:n.644-96_644-95insTTTTGAGACGGAGTCTCGCTCTGTCGCC...
NM_000789.4:c.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG MANE Select NP_000780.1:n.2306-96_2306-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCC...
NM_001178057.2:c.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG NP_001171528.1:n.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCC...
NM_152830.3:c.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG NP_690043.1:n.584-96_584-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAG...
NM_001382700.1:c.1739-96_1739-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG NP_001369629.1:n.1739-96_1739-95insTTTTGAGACGGAGTCTCGCTCTGTCG...
NM_001382701.1:c.1454-96_1454-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG NP_001369630.1:n.1454-96_1454-95insTTTTGAGACGGAGTCTCGCTCTGTCG...
NM_001382702.1:c.236-96_236-95insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG NP_001369631.1:n.236-96_236-95insTTTTGAGACGGAGTCTCGCTCTGTCGCC...
NR_168483.1:n.606-18_606-17insTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGG