Canonical Allele Identifier: CA2639246141

Gene: ACE

Linked Data

• gnomAD v4: 17-63498176-G-GATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498176_63498177insATCT , CM000679.2:g.63498176_63498177insATCT	GRCh38
NC_000017.10:g.61575537_61575538insATCT , CM000679.1:g.61575537_61575538insATCT	GRCh37
NC_000017.9:g.58929269_58929270insATCT	NCBI36
NG_011648.1:g.26104_26105insATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*810_*811insATCT MANE Select	ENSP00000290866.4:n.*810_*811insATCT
ENST00000290866.9:c.*810_*811insATCT	ENSP00000290866.4:n.*810_*811insATCT
ENST00000428043.5:c.*1153_*1154insATCT	ENSP00000397593.2:n.*1153_*1154insATCT
ENST00000577647.2:c.1969+1191_1969+1192insATCT	ENSP00000464149.1:n.1969+1191_1969+1192insATCT
NM_000789.3:c.*810_*811insATCT	NP_000780.1:n.*810_*811insATCT
NM_001178057.1:c.*810_*811insATCT	NP_001171528.1:n.*810_*811insATCT
NM_152830.2:c.*810_*811insATCT	NP_690043.1:n.*810_*811insATCT
XM_005257110.1:c.*810_*811insATCT	XP_005257167.1:n.*810_*811insATCT
XM_006721737.2:c.*810_*811insATCT	XP_006721800.2:n.*810_*811insATCT
NM_000789.4:c.*810_*811insATCT MANE Select	NP_000780.1:n.*810_*811insATCT
NM_001178057.2:c.*810_*811insATCT	NP_001171528.1:n.*810_*811insATCT
NM_152830.3:c.*810_*811insATCT	NP_690043.1:n.*810_*811insATCT
NM_001382700.1:c.*810_*811insATCT	NP_001369629.1:n.*810_*811insATCT
NM_001382701.1:c.*810_*811insATCT	NP_001369630.1:n.*810_*811insATCT
NM_001382702.1:c.*810_*811insATCT	NP_001369631.1:n.*810_*811insATCT
NR_168483.1:n.3109_3110insATCT