Canonical Allele Identifier: CA2269941713
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63480880G= , CM000679.2:g.63480880G= GRCh38
NC_000017.10:g.61558241G= , CM000679.1:g.61558241G= GRCh37
NC_000017.9:g.58911973G= NCBI36
NG_011648.1:g.8808G=

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.848-211G= MANE Select ENSP00000290866.4:n.848-211G=
ENST00000290866.9:c.848-211G= ENSP00000290866.4:n.848-211G=
ENST00000428043.5:c.848-211G= ENSP00000397593.2:n.848-211G=
ENST00000582627.1:c.848-211G= ENSP00000462280.1:n.848-211G=
ENST00000582678.5:c.*247-211G= ENSP00000462995.1:n.*247-211G=
ENST00000584529.5:n.882-211G=
NM_000789.3:c.848-211G= NP_000780.1:n.848-211G=
XM_005257110.1:c.299-211G= XP_005257167.1:n.299-211G=
NM_000789.4:c.848-211G= MANE Select NP_000780.1:n.848-211G=
NM_001382700.1:c.375-211G= NP_001369629.1:n.375-211G=
NM_001382701.1:c.-5-211G= NP_001369630.1:n.-5-211G=