Canonical Allele Identifier: CA773960764
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1282865358
MyVariant Identifiers: chr17:g.61558090_61558091insG (hg19) chr17:g.63480729_63480730insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63480732dup , CM000679.2:g.63480732dup GRCh38
NC_000017.10:g.61558093dup , CM000679.1:g.61558093dup GRCh37
NC_000017.9:g.58911825dup NCBI36
NG_011648.1:g.8660dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.847+204dup MANE Select ENSP00000290866.4:n.847+204dup
ENST00000290866.9:c.847+204dup ENSP00000290866.4:n.847+204dup
ENST00000428043.5:c.847+204dup ENSP00000397593.2:n.847+204dup
ENST00000582627.1:c.847+204dup ENSP00000462280.1:n.847+204dup
ENST00000582678.5:c.*246+204dup ENSP00000462995.1:n.*246+204dup
ENST00000584529.5:n.881+204dup
NM_000789.3:c.847+204dup NP_000780.1:n.847+204dup
XM_005257110.1:c.298+204dup XP_005257167.1:n.298+204dup
NM_000789.4:c.847+204dup MANE Select NP_000780.1:n.847+204dup
NM_001382700.1:c.374+204dup NP_001369629.1:n.374+204dup
NM_001382701.1:c.-6+204dup NP_001369630.1:n.-6+204dup
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