Canonical Allele Identifier: CA400567591

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574299A>C (hg19) ; chr17:g.63496938A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496938A>C , CM000679.2:g.63496938A>C	GRCh38
NC_000017.10:g.61574299A>C , CM000679.1:g.61574299A>C	GRCh37
NC_000017.9:g.58928031A>C	NCBI36
NG_011648.1:g.24866A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3644A>C MANE Select	ENSP00000290866.4:p.His1215Pro
ENST00000290863.10:c.1922A>C	ENSP00000290863.6:p.His641Pro
ENST00000290866.9:c.3644A>C	ENSP00000290866.4:p.His1215Pro
ENST00000413513.7:c.1799A>C	ENSP00000392247.3:p.His600Pro
ENST00000428043.5:c.3644A>C	ENSP00000397593.2:p.His1215Pro
ENST00000577418.5:n.654A>C
ENST00000577647.2:c.1922A>C	ENSP00000464149.1:p.His641Pro
ENST00000578839.5:c.*1399A>C	ENSP00000462110.2:n.*1399A>C
ENST00000579314.5:c.*1373A>C	ENSP00000462599.1:n.*1373A>C
ENST00000579409.1:c.331A>C
ENST00000582244.1:n.518A>C
NM_000789.3:c.3644A>C	NP_000780.1:p.His1215Pro
NM_001178057.1:c.1799A>C	NP_001171528.1:p.His600Pro
NM_152830.2:c.1922A>C	NP_690043.1:p.His641Pro
XM_005257110.1:c.3095A>C	XP_005257167.1:p.His1032Pro
XM_006721737.2:c.1982A>C	XP_006721800.2:p.His661Pro
XM_006721737.3:c.1982A>C	XP_006721800.2:p.His661Pro
NM_000789.4:c.3644A>C MANE Select	NP_000780.1:p.His1215Pro
NM_001178057.2:c.1799A>C	NP_001171528.1:p.His600Pro
NM_152830.3:c.1922A>C	NP_690043.1:p.His641Pro
NM_001382700.1:c.3077A>C	NP_001369629.1:p.His1026Pro
NM_001382701.1:c.2792A>C	NP_001369630.1:p.His931Pro
NM_001382702.1:c.1259A>C	NP_001369631.1:p.His420Pro
NR_168483.1:n.2022A>C