Canonical Allele Identifier: CA400569487

Gene: ACE

Linked Data

• dbSNP Id: rs2030826063
• MyVariant Identifiers: chr17:g.61574678A>C (hg19) ; chr17:g.63497317A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497317A>C , CM000679.2:g.63497317A>C	GRCh38
NC_000017.10:g.61574678A>C , CM000679.1:g.61574678A>C	GRCh37
NC_000017.9:g.58928410A>C	NCBI36
NG_011648.1:g.25245A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3872A>C MANE Select	ENSP00000290866.4:p.His1291Pro
ENST00000290863.10:c.2150A>C	ENSP00000290863.6:p.His717Pro
ENST00000290866.9:c.3872A>C	ENSP00000290866.4:p.His1291Pro
ENST00000413513.7:c.2027A>C	ENSP00000392247.3:p.His676Pro
ENST00000428043.5:c.*294A>C	ENSP00000397593.2:n.*294A>C
ENST00000577647.2:c.1969+332A>C	ENSP00000464149.1:n.1969+332A>C
ENST00000578839.5:c.*1627A>C	ENSP00000462110.2:n.*1627A>C
ENST00000579314.5:c.*1601A>C	ENSP00000462599.1:n.*1601A>C
NM_000789.3:c.3872A>C	NP_000780.1:p.His1291Pro
NM_001178057.1:c.2027A>C	NP_001171528.1:p.His676Pro
NM_152830.2:c.2150A>C	NP_690043.1:p.His717Pro
XM_005257110.1:c.3323A>C	XP_005257167.1:p.His1108Pro
XM_006721737.2:c.2210A>C	XP_006721800.2:p.His737Pro
XM_006721737.3:c.2210A>C	XP_006721800.2:p.His737Pro
NM_000789.4:c.3872A>C MANE Select	NP_000780.1:p.His1291Pro
NM_001178057.2:c.2027A>C	NP_001171528.1:p.His676Pro
NM_152830.3:c.2150A>C	NP_690043.1:p.His717Pro
NM_001382700.1:c.3305A>C	NP_001369629.1:p.His1102Pro
NM_001382701.1:c.3020A>C	NP_001369630.1:p.His1007Pro
NM_001382702.1:c.1487A>C	NP_001369631.1:p.His496Pro
NR_168483.1:n.2250A>C