Canonical Allele Identifier: CA2269950656

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498293_63498295delinsCTT , CM000679.2:g.63498293_63498295delinsCTT	GRCh38
NC_000017.10:g.61575654_61575656delinsCTT , CM000679.1:g.61575654_61575656delinsCTT	GRCh37
NC_000017.9:g.58929386_58929388delinsCTT	NCBI36
NG_011648.1:g.26221_26223delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*927_*929delinsCTT MANE Select	ENSP00000290866.4:n.*927_*929delinsCTT
ENST00000290866.9:c.*927_*929delinsCTT	ENSP00000290866.4:n.*927_*929delinsCTT
ENST00000428043.5:c.*1270_*1272delinsCTT	ENSP00000397593.2:n.*1270_*1272delinsCTT
ENST00000577647.2:c.1969+1308_1969+1310delinsCTT	ENSP00000464149.1:n.1969+1308_1969+1310delinsCTT
NM_000789.3:c.*927_*929delinsCTT	NP_000780.1:n.*927_*929delinsCTT
NM_001178057.1:c.*927_*929delinsCTT	NP_001171528.1:n.*927_*929delinsCTT
NM_152830.2:c.*927_*929delinsCTT	NP_690043.1:n.*927_*929delinsCTT
XM_005257110.1:c.*927_*929delinsCTT	XP_005257167.1:n.*927_*929delinsCTT
XM_006721737.2:c.*927_*929delinsCTT	XP_006721800.2:n.*927_*929delinsCTT
NM_000789.4:c.*927_*929delinsCTT MANE Select	NP_000780.1:n.*927_*929delinsCTT
NM_001178057.2:c.*927_*929delinsCTT	NP_001171528.1:n.*927_*929delinsCTT
NM_152830.3:c.*927_*929delinsCTT	NP_690043.1:n.*927_*929delinsCTT
NM_001382700.1:c.*927_*929delinsCTT	NP_001369629.1:n.*927_*929delinsCTT
NM_001382701.1:c.*927_*929delinsCTT	NP_001369630.1:n.*927_*929delinsCTT
NM_001382702.1:c.*927_*929delinsCTT	NP_001369631.1:n.*927_*929delinsCTT
NR_168483.1:n.3226_3228delinsCTT