Canonical Allele Identifier: CA2733906495

Gene: ACE

Linked Data

• dbSNP Id: rs2147583223

Genomic Alleles

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

Transcript Alleles

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