Canonical Allele Identifier: CA2639245406

Gene: ACE

Linked Data

• gnomAD v4: 17-63497922-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497922A>G , CM000679.2:g.63497922A>G	GRCh38
NC_000017.10:g.61575283A>G , CM000679.1:g.61575283A>G	GRCh37
NC_000017.9:g.58929015A>G	NCBI36
NG_011648.1:g.25850A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*556A>G MANE Select	ENSP00000290866.4:n.*556A>G
ENST00000290866.9:c.*556A>G	ENSP00000290866.4:n.*556A>G
ENST00000428043.5:c.*899A>G	ENSP00000397593.2:n.*899A>G
ENST00000577647.2:c.1969+937A>G	ENSP00000464149.1:n.1969+937A>G
NM_000789.3:c.*556A>G	NP_000780.1:n.*556A>G
NM_001178057.1:c.*556A>G	NP_001171528.1:n.*556A>G
NM_152830.2:c.*556A>G	NP_690043.1:n.*556A>G
XM_005257110.1:c.*556A>G	XP_005257167.1:n.*556A>G
XM_006721737.2:c.*556A>G	XP_006721800.2:n.*556A>G
NM_000789.4:c.*556A>G MANE Select	NP_000780.1:n.*556A>G
NM_001178057.2:c.*556A>G	NP_001171528.1:n.*556A>G
NM_152830.3:c.*556A>G	NP_690043.1:n.*556A>G
NM_001382700.1:c.*556A>G	NP_001369629.1:n.*556A>G
NM_001382701.1:c.*556A>G	NP_001369630.1:n.*556A>G
NM_001382702.1:c.*556A>G	NP_001369631.1:n.*556A>G
NR_168483.1:n.2855A>G