Canonical Allele Identifier: CA400557856
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488683G>A , CM000679.2:g.63488683G>A GRCh38
NC_000017.10:g.61566044G>A , CM000679.1:g.61566044G>A GRCh37
NC_000017.9:g.58919776G>A NCBI36
NG_011648.1:g.16611G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2341G>A MANE Select ENSP00000290866.4:p.Glu781Lys
ENST00000290863.10:c.619G>A ENSP00000290863.6:p.Glu207Lys
ENST00000290866.9:c.2341G>A ENSP00000290866.4:p.Glu781Lys
ENST00000413513.7:c.619G>A ENSP00000392247.3:p.Glu207Lys
ENST00000428043.5:c.2341G>A ENSP00000397593.2:p.Glu781Lys
ENST00000577647.2:c.619G>A ENSP00000464149.1:p.Glu207Lys
ENST00000578839.5:c.*411G>A ENSP00000462110.2:n.*411G>A
ENST00000579204.1:c.600G>A ENSP00000464629.1:n.600G>A
ENST00000579314.5:c.*70G>A ENSP00000462599.1:n.*70G>A
ENST00000582005.5:c.*261G>A ENSP00000462002.1:n.*261G>A
ENST00000582761.1:c.109G>A ENSP00000462909.1:p.Glu37Lys
ENST00000584865.5:n.287G>A
NM_000789.3:c.2341G>A NP_000780.1:p.Glu781Lys
NM_001178057.1:c.619G>A NP_001171528.1:p.Glu207Lys
NM_152830.2:c.619G>A NP_690043.1:p.Glu207Lys
XM_005257110.1:c.1792G>A XP_005257167.1:p.Glu598Lys
XM_006721737.2:c.679G>A XP_006721800.2:p.Glu227Lys
XM_006721737.3:c.679G>A XP_006721800.2:p.Glu227Lys
NM_000789.4:c.2341G>A MANE Select NP_000780.1:p.Glu781Lys
NM_001178057.2:c.619G>A NP_001171528.1:p.Glu207Lys
NM_152830.3:c.619G>A NP_690043.1:p.Glu207Lys
NM_001382700.1:c.1774G>A NP_001369629.1:p.Glu592Lys
NM_001382701.1:c.1489G>A NP_001369630.1:p.Glu497Lys
NM_001382702.1:c.271G>A NP_001369631.1:p.Glu91Lys
NR_168483.1:n.719G>A