Canonical Allele Identifier: CA400539551
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477626A>C , CM000679.2:g.63477626A>C GRCh38
NC_000017.10:g.61554987A>C , CM000679.1:g.61554987A>C GRCh37
NC_000017.9:g.58908719A>C NCBI36
NG_011648.1:g.5554A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.249+283A>C MANE Select ENSP00000290866.4:n.249+283A>C
ENST00000290866.9:c.249+283A>C ENSP00000290866.4:n.249+283A>C
ENST00000428043.5:c.249+283A>C ENSP00000397593.2:n.249+283A>C
ENST00000579462.1:n.274+283A>C
ENST00000580318.1:n.134A>C
ENST00000582627.1:c.85A>C ENSP00000462280.1:p.Ser29Arg
ENST00000582678.5:c.249+283A>C ENSP00000462995.1:n.249+283A>C
ENST00000583336.5:n.283+283A>C
ENST00000584529.5:n.283+283A>C
NM_000789.3:c.249+283A>C NP_000780.1:n.249+283A>C
XM_005257110.1:c.-207+283A>C XP_005257167.1:n.-207+283A>C
NM_000789.4:c.249+283A>C MANE Select NP_000780.1:n.249+283A>C
NM_001382700.1:c.14+283A>C NP_001369629.1:n.14+283A>C
NM_001382701.1:c.-366+283A>C NP_001369630.1:n.-366+283A>C