Canonical Allele Identifier: CA985400094

Gene: ACE

Linked Data

• dbSNP Id: rs2030883744
• gnomAD v4: 17-63498045-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498045C>A , CM000679.2:g.63498045C>A	GRCh38
NC_000017.10:g.61575406C>A , CM000679.1:g.61575406C>A	GRCh37
NC_000017.9:g.58929138C>A	NCBI36
NG_011648.1:g.25973C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*679C>A MANE Select	ENSP00000290866.4:n.*679C>A
ENST00000290866.9:c.*679C>A	ENSP00000290866.4:n.*679C>A
ENST00000428043.5:c.*1022C>A	ENSP00000397593.2:n.*1022C>A
ENST00000577647.2:c.1969+1060C>A	ENSP00000464149.1:n.1969+1060C>A
NM_000789.3:c.*679C>A	NP_000780.1:n.*679C>A
NM_001178057.1:c.*679C>A	NP_001171528.1:n.*679C>A
NM_152830.2:c.*679C>A	NP_690043.1:n.*679C>A
XM_005257110.1:c.*679C>A	XP_005257167.1:n.*679C>A
XM_006721737.2:c.*679C>A	XP_006721800.2:n.*679C>A
NM_000789.4:c.*679C>A MANE Select	NP_000780.1:n.*679C>A
NM_001178057.2:c.*679C>A	NP_001171528.1:n.*679C>A
NM_152830.3:c.*679C>A	NP_690043.1:n.*679C>A
NM_001382700.1:c.*679C>A	NP_001369629.1:n.*679C>A
NM_001382701.1:c.*679C>A	NP_001369630.1:n.*679C>A
NM_001382702.1:c.*679C>A	NP_001369631.1:n.*679C>A
NR_168483.1:n.2978C>A