Canonical Allele Identifier: CA14383515
Gene: ACE HGNC NCBI

Linked Data

ClinVar Variation Id: 1278455
ClinVar RCV Id: RCV001688063
dbSNP Id: rs4305

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63480868A>G , CM000679.2:g.63480868A>G GRCh38
NC_000017.10:g.61558229A>G , CM000679.1:g.61558229A>G GRCh37
NC_000017.9:g.58911961A>G NCBI36
NG_011648.1:g.8796A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.848-223A>G MANE Select ENSP00000290866.4:n.848-223A>G
ENST00000290866.9:c.848-223A>G ENSP00000290866.4:n.848-223A>G
ENST00000428043.5:c.848-223A>G ENSP00000397593.2:n.848-223A>G
ENST00000582627.1:c.848-223A>G ENSP00000462280.1:n.848-223A>G
ENST00000582678.5:c.*247-223A>G ENSP00000462995.1:n.*247-223A>G
ENST00000584529.5:n.882-223A>G
NM_000789.3:c.848-223A>G NP_000780.1:n.848-223A>G
XM_005257110.1:c.299-223A>G XP_005257167.1:n.299-223A>G
NM_000789.4:c.848-223A>G MANE Select NP_000780.1:n.848-223A>G
NM_001382700.1:c.375-223A>G NP_001369629.1:n.375-223A>G
NM_001382701.1:c.-5-223A>G NP_001369630.1:n.-5-223A>G