Canonical Allele Identifier: CA2639246341

Gene: ACE

Linked Data

• gnomAD v4: 17-63498236-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498236_63498237insT , CM000679.2:g.63498236_63498237insT	GRCh38
NC_000017.10:g.61575597_61575598insT , CM000679.1:g.61575597_61575598insT	GRCh37
NC_000017.9:g.58929329_58929330insT	NCBI36
NG_011648.1:g.26164_26165insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*870_*871insT MANE Select	ENSP00000290866.4:n.*870_*871insT
ENST00000290866.9:c.*870_*871insT	ENSP00000290866.4:n.*870_*871insT
ENST00000428043.5:c.*1213_*1214insT	ENSP00000397593.2:n.*1213_*1214insT
ENST00000577647.2:c.1969+1251_1969+1252insT	ENSP00000464149.1:n.1969+1251_1969+1252insT
NM_000789.3:c.*870_*871insT	NP_000780.1:n.*870_*871insT
NM_001178057.1:c.*870_*871insT	NP_001171528.1:n.*870_*871insT
NM_152830.2:c.*870_*871insT	NP_690043.1:n.*870_*871insT
XM_005257110.1:c.*870_*871insT	XP_005257167.1:n.*870_*871insT
XM_006721737.2:c.*870_*871insT	XP_006721800.2:n.*870_*871insT
NM_000789.4:c.*870_*871insT MANE Select	NP_000780.1:n.*870_*871insT
NM_001178057.2:c.*870_*871insT	NP_001171528.1:n.*870_*871insT
NM_152830.3:c.*870_*871insT	NP_690043.1:n.*870_*871insT
NM_001382700.1:c.*870_*871insT	NP_001369629.1:n.*870_*871insT
NM_001382701.1:c.*870_*871insT	NP_001369630.1:n.*870_*871insT
NM_001382702.1:c.*870_*871insT	NP_001369631.1:n.*870_*871insT
NR_168483.1:n.3169_3170insT