Canonical Allele Identifier: CA627147986

Gene: ACE

Linked Data

• dbSNP Id: rs1350820565
• gnomAD v2: 17-61574152-TC-T
• gnomAD v4: 17-63496791-TC-T
• MyVariant Identifiers: chr17:g.61574153del (hg19) ; chr17:g.63496792del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496795del , CM000679.2:g.63496795del	GRCh38
NC_000017.10:g.61574156del , CM000679.1:g.61574156del	GRCh37
NC_000017.9:g.58927888del	NCBI36
NG_011648.1:g.24723del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3504-3del MANE Select	ENSP00000290866.4:n.3504-3del
ENST00000290863.10:c.1782-3del	ENSP00000290863.6:n.1782-3del
ENST00000290866.9:c.3504-3del	ENSP00000290866.4:n.3504-3del
ENST00000413513.7:c.1659-3del	ENSP00000392247.3:n.1659-3del
ENST00000428043.5:c.3504-3del	ENSP00000397593.2:n.3504-3del
ENST00000577418.5:n.514-3del
ENST00000577647.2:c.1782-3del	ENSP00000464149.1:n.1782-3del
ENST00000578839.5:c.*1259-3del	ENSP00000462110.2:n.*1259-3del
ENST00000579314.5:c.*1233-3del	ENSP00000462599.1:n.*1233-3del
ENST00000579409.1:c.191-3del
ENST00000582244.1:n.378-3del
NM_000789.3:c.3504-3del	NP_000780.1:n.3504-3del
NM_001178057.1:c.1659-3del	NP_001171528.1:n.1659-3del
NM_152830.2:c.1782-3del	NP_690043.1:n.1782-3del
XM_005257110.1:c.2955-3del	XP_005257167.1:n.2955-3del
XM_006721737.2:c.1842-3del	XP_006721800.2:n.1842-3del
XM_006721737.3:c.1842-3del	XP_006721800.2:n.1842-3del
NM_000789.4:c.3504-3del MANE Select	NP_000780.1:n.3504-3del
NM_001178057.2:c.1659-3del	NP_001171528.1:n.1659-3del
NM_152830.3:c.1782-3del	NP_690043.1:n.1782-3del
NM_001382700.1:c.2937-3del	NP_001369629.1:n.2937-3del
NM_001382701.1:c.2652-3del	NP_001369630.1:n.2652-3del
NM_001382702.1:c.1119-3del	NP_001369631.1:n.1119-3del
NR_168483.1:n.1882-3del