Canonical Allele Identifier: CA400566959

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574221A>C (hg19) ; chr17:g.63496860A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496860A>C , CM000679.2:g.63496860A>C	GRCh38
NC_000017.10:g.61574221A>C , CM000679.1:g.61574221A>C	GRCh37
NC_000017.9:g.58927953A>C	NCBI36
NG_011648.1:g.24788A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3566A>C MANE Select	ENSP00000290866.4:p.Gln1189Pro
ENST00000290863.10:c.1844A>C	ENSP00000290863.6:p.Gln615Pro
ENST00000290866.9:c.3566A>C	ENSP00000290866.4:p.Gln1189Pro
ENST00000413513.7:c.1721A>C	ENSP00000392247.3:p.Gln574Pro
ENST00000428043.5:c.3566A>C	ENSP00000397593.2:p.Gln1189Pro
ENST00000577418.5:n.576A>C
ENST00000577647.2:c.1844A>C	ENSP00000464149.1:p.Gln615Pro
ENST00000578839.5:c.*1321A>C	ENSP00000462110.2:n.*1321A>C
ENST00000579314.5:c.*1295A>C	ENSP00000462599.1:n.*1295A>C
ENST00000579409.1:c.253A>C
ENST00000582244.1:n.440A>C
NM_000789.3:c.3566A>C	NP_000780.1:p.Gln1189Pro
NM_001178057.1:c.1721A>C	NP_001171528.1:p.Gln574Pro
NM_152830.2:c.1844A>C	NP_690043.1:p.Gln615Pro
XM_005257110.1:c.3017A>C	XP_005257167.1:p.Gln1006Pro
XM_006721737.2:c.1904A>C	XP_006721800.2:p.Gln635Pro
XM_006721737.3:c.1904A>C	XP_006721800.2:p.Gln635Pro
NM_000789.4:c.3566A>C MANE Select	NP_000780.1:p.Gln1189Pro
NM_001178057.2:c.1721A>C	NP_001171528.1:p.Gln574Pro
NM_152830.3:c.1844A>C	NP_690043.1:p.Gln615Pro
NM_001382700.1:c.2999A>C	NP_001369629.1:p.Gln1000Pro
NM_001382701.1:c.2714A>C	NP_001369630.1:p.Gln905Pro
NM_001382702.1:c.1181A>C	NP_001369631.1:p.Gln394Pro
NR_168483.1:n.1944A>C