Canonical Allele Identifier: CA2269943114
Gene: ACE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483427_63483428delinsAG , CM000679.2:g.63483427_63483428delinsAG GRCh38
NC_000017.10:g.61560788_61560789delinsAG , CM000679.1:g.61560788_61560789delinsAG GRCh37
NC_000017.9:g.58914520_58914521delinsAG NCBI36
NG_011648.1:g.11355_11356delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1488-33_1488-32delinsAG MANE Select ENSP00000290866.4:n.1488-33_1488-32delins...
ENST00000290866.9:c.1488-33_1488-32delinsAG ENSP00000290866.4:n.1488-33_1488-32delins...
ENST00000428043.5:c.1488-33_1488-32delinsAG ENSP00000397593.2:n.1488-33_1488-32delins...
ENST00000582678.5:c.*887-33_*887-32delinsAG ENSP00000462995.1:n.*887-33_*887-32delins...
ENST00000584529.5:n.1377-33_1377-32delinsAG
NM_000789.3:c.1488-33_1488-32delinsAG NP_000780.1:n.1488-33_1488-32delinsAG
XM_005257110.1:c.939-33_939-32delinsAG XP_005257167.1:n.939-33_939-32delinsAG
NM_000789.4:c.1488-33_1488-32delinsAG MANE Select NP_000780.1:n.1488-33_1488-32delinsAG
NM_001382700.1:c.921-33_921-32delinsAG NP_001369629.1:n.921-33_921-32delinsAG
NM_001382701.1:c.636-33_636-32delinsAG NP_001369630.1:n.636-33_636-32delinsAG
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