Canonical Allele Identifier: CA2639246217

Gene: ACE

Linked Data

• gnomAD v4: 17-63498193-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498193_63498194insT , CM000679.2:g.63498193_63498194insT	GRCh38
NC_000017.10:g.61575554_61575555insT , CM000679.1:g.61575554_61575555insT	GRCh37
NC_000017.9:g.58929286_58929287insT	NCBI36
NG_011648.1:g.26121_26122insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*827_*828insT MANE Select	ENSP00000290866.4:n.*827_*828insT
ENST00000290866.9:c.*827_*828insT	ENSP00000290866.4:n.*827_*828insT
ENST00000428043.5:c.*1170_*1171insT	ENSP00000397593.2:n.*1170_*1171insT
ENST00000577647.2:c.1969+1208_1969+1209insT	ENSP00000464149.1:n.1969+1208_1969+1209insT
NM_000789.3:c.*827_*828insT	NP_000780.1:n.*827_*828insT
NM_001178057.1:c.*827_*828insT	NP_001171528.1:n.*827_*828insT
NM_152830.2:c.*827_*828insT	NP_690043.1:n.*827_*828insT
XM_005257110.1:c.*827_*828insT	XP_005257167.1:n.*827_*828insT
XM_006721737.2:c.*827_*828insT	XP_006721800.2:n.*827_*828insT
NM_000789.4:c.*827_*828insT MANE Select	NP_000780.1:n.*827_*828insT
NM_001178057.2:c.*827_*828insT	NP_001171528.1:n.*827_*828insT
NM_152830.3:c.*827_*828insT	NP_690043.1:n.*827_*828insT
NM_001382700.1:c.*827_*828insT	NP_001369629.1:n.*827_*828insT
NM_001382701.1:c.*827_*828insT	NP_001369630.1:n.*827_*828insT
NM_001382702.1:c.*827_*828insT	NP_001369631.1:n.*827_*828insT
NR_168483.1:n.3126_3127insT