Canonical Allele Identifier: CA773988970
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1356935333

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477675_63477679dup , CM000679.2:g.63477675_63477679dup GRCh38
NC_000017.10:g.61555036_61555040dup , CM000679.1:g.61555036_61555040dup GRCh37
NC_000017.9:g.58908768_58908772dup NCBI36
NG_011648.1:g.5603_5607dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.250-256_250-252dup MANE Select ENSP00000290866.4:n.250-256_250-252dup
ENST00000290866.9:c.250-256_250-252dup ENSP00000290866.4:n.250-256_250-252dup
ENST00000428043.5:c.250-256_250-252dup ENSP00000397593.2:n.250-256_250-252dup
ENST00000579462.1:n.275-256_275-252dup
ENST00000580318.1:n.183_187dup
ENST00000582627.1:c.134_138dup ENSP00000462280.1:p.Ser47HisfsTer?
ENST00000582678.5:c.250-256_250-252dup ENSP00000462995.1:n.250-256_250-252dup
ENST00000583336.5:n.284-256_284-252dup
ENST00000584529.5:n.284-256_284-252dup
NM_000789.3:c.250-256_250-252dup NP_000780.1:n.250-256_250-252dup
XM_005257110.1:c.-206-256_-206-252dup XP_005257167.1:n.-206-256_-206-252dup
NM_000789.4:c.250-256_250-252dup MANE Select NP_000780.1:n.250-256_250-252dup
NM_001382700.1:c.15-256_15-252dup NP_001369629.1:n.15-256_15-252dup
NM_001382701.1:c.-365-256_-365-252dup NP_001369630.1:n.-365-256_-365-252dup