Canonical Allele Identifier: CA2269939893
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477262C= , CM000679.2:g.63477262C= GRCh38
NC_000017.10:g.61554623C= , CM000679.1:g.61554623C= GRCh37
NC_000017.9:g.58908355C= NCBI36
NG_011648.1:g.5190C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.168C= MANE Select ENSP00000290866.4:p.Ser56=
ENST00000290866.9:c.168C= ENSP00000290866.4:p.Ser56=
ENST00000428043.5:c.168C= ENSP00000397593.2:p.Ser56=
ENST00000579462.1:n.193C=
ENST00000582678.5:c.168C= ENSP00000462995.1:p.Ser56=
ENST00000583336.5:n.202C=
ENST00000584529.5:n.202C=
NM_000789.3:c.168C= NP_000780.1:p.Ser56=
XM_005257110.1:c.-288C= XP_005257167.1:n.-288C=
NM_000789.4:c.168C= MANE Select NP_000780.1:p.Ser56=
NM_001382700.1:c.-68C= NP_001369629.1:n.-68C=
NM_001382701.1:c.-447C= NP_001369630.1:n.-447C=