Canonical Allele Identifier: CA400566828

Gene: ACE

Linked Data

• gnomAD v4: 17-63496845-A-C
• MyVariant Identifiers: chr17:g.61574206A>C (hg19) ; chr17:g.63496845A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496845A>C , CM000679.2:g.63496845A>C	GRCh38
NC_000017.10:g.61574206A>C , CM000679.1:g.61574206A>C	GRCh37
NC_000017.9:g.58927938A>C	NCBI36
NG_011648.1:g.24773A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3551A>C MANE Select	ENSP00000290866.4:p.Gln1184Pro
ENST00000290863.10:c.1829A>C	ENSP00000290863.6:p.Gln610Pro
ENST00000290866.9:c.3551A>C	ENSP00000290866.4:p.Gln1184Pro
ENST00000413513.7:c.1706A>C	ENSP00000392247.3:p.Gln569Pro
ENST00000428043.5:c.3551A>C	ENSP00000397593.2:p.Gln1184Pro
ENST00000577418.5:n.561A>C
ENST00000577647.2:c.1829A>C	ENSP00000464149.1:p.Gln610Pro
ENST00000578839.5:c.*1306A>C	ENSP00000462110.2:n.*1306A>C
ENST00000579314.5:c.*1280A>C	ENSP00000462599.1:n.*1280A>C
ENST00000579409.1:c.238A>C
ENST00000582244.1:n.425A>C
NM_000789.3:c.3551A>C	NP_000780.1:p.Gln1184Pro
NM_001178057.1:c.1706A>C	NP_001171528.1:p.Gln569Pro
NM_152830.2:c.1829A>C	NP_690043.1:p.Gln610Pro
XM_005257110.1:c.3002A>C	XP_005257167.1:p.Gln1001Pro
XM_006721737.2:c.1889A>C	XP_006721800.2:p.Gln630Pro
XM_006721737.3:c.1889A>C	XP_006721800.2:p.Gln630Pro
NM_000789.4:c.3551A>C MANE Select	NP_000780.1:p.Gln1184Pro
NM_001178057.2:c.1706A>C	NP_001171528.1:p.Gln569Pro
NM_152830.3:c.1829A>C	NP_690043.1:p.Gln610Pro
NM_001382700.1:c.2984A>C	NP_001369629.1:p.Gln995Pro
NM_001382701.1:c.2699A>C	NP_001369630.1:p.Gln900Pro
NM_001382702.1:c.1166A>C	NP_001369631.1:p.Gln389Pro
NR_168483.1:n.1929A>C