Canonical Allele Identifier: CA400567741

Gene: ACE

Linked Data

• gnomAD v4: 17-63496961-C-A
• MyVariant Identifiers: chr17:g.61574322C>A (hg19) ; chr17:g.63496961C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496961C>A , CM000679.2:g.63496961C>A	GRCh38
NC_000017.10:g.61574322C>A , CM000679.1:g.61574322C>A	GRCh37
NC_000017.9:g.58928054C>A	NCBI36
NG_011648.1:g.24889C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3667C>A MANE Select	ENSP00000290866.4:p.Gln1223Lys
ENST00000290863.10:c.1945C>A	ENSP00000290863.6:p.Gln649Lys
ENST00000290866.9:c.3667C>A	ENSP00000290866.4:p.Gln1223Lys
ENST00000413513.7:c.1822C>A	ENSP00000392247.3:p.Gln608Lys
ENST00000428043.5:c.3667C>A	ENSP00000397593.2:p.Gln1223Lys
ENST00000577418.5:n.677C>A
ENST00000577647.2:c.1945C>A	ENSP00000464149.1:p.Gln649Lys
ENST00000578839.5:c.*1422C>A	ENSP00000462110.2:n.*1422C>A
ENST00000579314.5:c.*1396C>A	ENSP00000462599.1:n.*1396C>A
ENST00000579409.1:c.354C>A
ENST00000582244.1:n.541C>A
NM_000789.3:c.3667C>A	NP_000780.1:p.Gln1223Lys
NM_001178057.1:c.1822C>A	NP_001171528.1:p.Gln608Lys
NM_152830.2:c.1945C>A	NP_690043.1:p.Gln649Lys
XM_005257110.1:c.3118C>A	XP_005257167.1:p.Gln1040Lys
XM_006721737.2:c.2005C>A	XP_006721800.2:p.Gln669Lys
XM_006721737.3:c.2005C>A	XP_006721800.2:p.Gln669Lys
NM_000789.4:c.3667C>A MANE Select	NP_000780.1:p.Gln1223Lys
NM_001178057.2:c.1822C>A	NP_001171528.1:p.Gln608Lys
NM_152830.3:c.1945C>A	NP_690043.1:p.Gln649Lys
NM_001382700.1:c.3100C>A	NP_001369629.1:p.Gln1034Lys
NM_001382701.1:c.2815C>A	NP_001369630.1:p.Gln939Lys
NM_001382702.1:c.1282C>A	NP_001369631.1:p.Gln428Lys
NR_168483.1:n.2045C>A