Canonical Allele Identifier: CA400539462
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477602T>A , CM000679.2:g.63477602T>A GRCh38
NC_000017.10:g.61554963T>A , CM000679.1:g.61554963T>A GRCh37
NC_000017.9:g.58908695T>A NCBI36
NG_011648.1:g.5530T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.249+259T>A MANE Select ENSP00000290866.4:n.249+259T>A
ENST00000290866.9:c.249+259T>A ENSP00000290866.4:n.249+259T>A
ENST00000428043.5:c.249+259T>A ENSP00000397593.2:n.249+259T>A
ENST00000579462.1:n.274+259T>A
ENST00000580318.1:n.110T>A
ENST00000582627.1:c.61T>A ENSP00000462280.1:p.Ser21Thr
ENST00000582678.5:c.249+259T>A ENSP00000462995.1:n.249+259T>A
ENST00000583336.5:n.283+259T>A
ENST00000584529.5:n.283+259T>A
NM_000789.3:c.249+259T>A NP_000780.1:n.249+259T>A
XM_005257110.1:c.-207+259T>A XP_005257167.1:n.-207+259T>A
NM_000789.4:c.249+259T>A MANE Select NP_000780.1:n.249+259T>A
NM_001382700.1:c.14+259T>A NP_001369629.1:n.14+259T>A
NM_001382701.1:c.-366+259T>A NP_001369630.1:n.-366+259T>A