Canonical Allele Identifier: CA2269941670
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs2049694358
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63480793A>C , CM000679.2:g.63480793A>C GRCh38
NC_000017.10:g.61558154A>C , CM000679.1:g.61558154A>C GRCh37
NC_000017.9:g.58911886A>C NCBI36
NG_011648.1:g.8721A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.847+265A>C MANE Select ENSP00000290866.4:n.847+265A>C
ENST00000290866.9:c.847+265A>C ENSP00000290866.4:n.847+265A>C
ENST00000428043.5:c.847+265A>C ENSP00000397593.2:n.847+265A>C
ENST00000582627.1:c.847+265A>C ENSP00000462280.1:n.847+265A>C
ENST00000582678.5:c.*246+265A>C ENSP00000462995.1:n.*246+265A>C
ENST00000584529.5:n.881+265A>C
NM_000789.3:c.847+265A>C NP_000780.1:n.847+265A>C
XM_005257110.1:c.298+265A>C XP_005257167.1:n.298+265A>C
NM_000789.4:c.847+265A>C MANE Select NP_000780.1:n.847+265A>C
NM_001382700.1:c.374+265A>C NP_001369629.1:n.374+265A>C
NM_001382701.1:c.-6+265A>C NP_001369630.1:n.-6+265A>C
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