Canonical Allele Identifier: CA919875963
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1599139720
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63480792dup , CM000679.2:g.63480792dup GRCh38
NC_000017.10:g.61558153dup , CM000679.1:g.61558153dup GRCh37
NC_000017.9:g.58911885dup NCBI36
NG_011648.1:g.8720dup

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.847+264dup MANE Select ENSP00000290866.4:n.847+264dup
ENST00000290866.9:c.847+264dup ENSP00000290866.4:n.847+264dup
ENST00000428043.5:c.847+264dup ENSP00000397593.2:n.847+264dup
ENST00000582627.1:c.847+264dup ENSP00000462280.1:n.847+264dup
ENST00000582678.5:c.*246+264dup ENSP00000462995.1:n.*246+264dup
ENST00000584529.5:n.881+264dup
NM_000789.3:c.847+264dup NP_000780.1:n.847+264dup
XM_005257110.1:c.298+264dup XP_005257167.1:n.298+264dup
NM_000789.4:c.847+264dup MANE Select NP_000780.1:n.847+264dup
NM_001382700.1:c.374+264dup NP_001369629.1:n.374+264dup
NM_001382701.1:c.-6+264dup NP_001369630.1:n.-6+264dup
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