Canonical Allele Identifier: CA627147964
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1454161732

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63497113G>T , CM000679.2:g.63497113G>T GRCh38
NC_000017.10:g.61574474G>T , CM000679.1:g.61574474G>T GRCh37
NC_000017.9:g.58928206G>T NCBI36
NG_011648.1:g.25041G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3692-24G>T MANE Select ENSP00000290866.4:n.3692-24G>T
ENST00000290863.10:c.1970-24G>T ENSP00000290863.6:n.1970-24G>T
ENST00000290866.9:c.3692-24G>T ENSP00000290866.4:n.3692-24G>T
ENST00000413513.7:c.1847-24G>T ENSP00000392247.3:n.1847-24G>T
ENST00000428043.5:c.*90G>T ENSP00000397593.2:n.*90G>T
ENST00000577418.5:n.702-24G>T
ENST00000577647.2:c.1969+128G>T ENSP00000464149.1:n.1969+128G>T
ENST00000578839.5:c.*1447-24G>T ENSP00000462110.2:n.*1447-24G>T
ENST00000579314.5:c.*1421-24G>T ENSP00000462599.1:n.*1421-24G>T
ENST00000579409.1:c.506G>T
NM_000789.3:c.3692-24G>T NP_000780.1:n.3692-24G>T
NM_001178057.1:c.1847-24G>T NP_001171528.1:n.1847-24G>T
NM_152830.2:c.1970-24G>T NP_690043.1:n.1970-24G>T
XM_005257110.1:c.3143-24G>T XP_005257167.1:n.3143-24G>T
XM_006721737.2:c.2030-24G>T XP_006721800.2:n.2030-24G>T
XM_006721737.3:c.2030-24G>T XP_006721800.2:n.2030-24G>T
NM_000789.4:c.3692-24G>T MANE Select NP_000780.1:n.3692-24G>T
NM_001178057.2:c.1847-24G>T NP_001171528.1:n.1847-24G>T
NM_152830.3:c.1970-24G>T NP_690043.1:n.1970-24G>T
NM_001382700.1:c.3125-24G>T NP_001369629.1:n.3125-24G>T
NM_001382701.1:c.2840-24G>T NP_001369630.1:n.2840-24G>T
NM_001382702.1:c.1307-24G>T NP_001369631.1:n.1307-24G>T
NR_168483.1:n.2070-24G>T