Canonical Allele Identifier: CA400568306
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1474601688

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63497143C>T , CM000679.2:g.63497143C>T GRCh38
NC_000017.10:g.61574504C>T , CM000679.1:g.61574504C>T GRCh37
NC_000017.9:g.58928236C>T NCBI36
NG_011648.1:g.25071C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3698C>T MANE Select ENSP00000290866.4:p.Ser1233Leu
ENST00000290863.10:c.1976C>T ENSP00000290863.6:p.Ser659Leu
ENST00000290866.9:c.3698C>T ENSP00000290866.4:p.Ser1233Leu
ENST00000413513.7:c.1853C>T ENSP00000392247.3:p.Ser618Leu
ENST00000428043.5:c.*120C>T ENSP00000397593.2:n.*120C>T
ENST00000577418.5:n.708C>T
ENST00000577647.2:c.1969+158C>T ENSP00000464149.1:n.1969+158C>T
ENST00000578839.5:c.*1453C>T ENSP00000462110.2:n.*1453C>T
ENST00000579314.5:c.*1427C>T ENSP00000462599.1:n.*1427C>T
ENST00000579409.1:c.536C>T
NM_000789.3:c.3698C>T NP_000780.1:p.Ser1233Leu
NM_001178057.1:c.1853C>T NP_001171528.1:p.Ser618Leu
NM_152830.2:c.1976C>T NP_690043.1:p.Ser659Leu
XM_005257110.1:c.3149C>T XP_005257167.1:p.Ser1050Leu
XM_006721737.2:c.2036C>T XP_006721800.2:p.Ser679Leu
XM_006721737.3:c.2036C>T XP_006721800.2:p.Ser679Leu
NM_000789.4:c.3698C>T MANE Select NP_000780.1:p.Ser1233Leu
NM_001178057.2:c.1853C>T NP_001171528.1:p.Ser618Leu
NM_152830.3:c.1976C>T NP_690043.1:p.Ser659Leu
NM_001382700.1:c.3131C>T NP_001369629.1:p.Ser1044Leu
NM_001382701.1:c.2846C>T NP_001369630.1:p.Ser949Leu
NM_001382702.1:c.1313C>T NP_001369631.1:p.Ser438Leu
NR_168483.1:n.2076C>T