Canonical Allele Identifier: CA2269939741
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477164C= , CM000679.2:g.63477164C= GRCh38
NC_000017.10:g.61554525C= , CM000679.1:g.61554525C= GRCh37
NC_000017.9:g.58908257C= NCBI36
NG_011648.1:g.5092C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.70C= MANE Select ENSP00000290866.4:p.Pro24=
ENST00000290866.9:c.70C= ENSP00000290866.4:p.Pro24=
ENST00000428043.5:c.70C= ENSP00000397593.2:p.Pro24=
ENST00000579462.1:n.95C=
ENST00000582678.5:c.70C= ENSP00000462995.1:p.Pro24=
ENST00000583336.5:n.104C=
ENST00000584529.5:n.104C=
NM_000789.3:c.70C= NP_000780.1:p.Pro24=
XM_005257110.1:c.-386C= XP_005257167.1:n.-386C=
NM_000789.4:c.70C= MANE Select NP_000780.1:p.Pro24=
NM_001382700.1:c.-166C= NP_001369629.1:n.-166C=
NM_001382701.1:c.-545C= NP_001369630.1:n.-545C=