Canonical Allele Identifier: CA2269950622

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498233_63498235delinsGCA , CM000679.2:g.63498233_63498235delinsGCA	GRCh38
NC_000017.10:g.61575594_61575596delinsGCA , CM000679.1:g.61575594_61575596delinsGCA	GRCh37
NC_000017.9:g.58929326_58929328delinsGCA	NCBI36
NG_011648.1:g.26161_26163delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*867_*869delinsGCA MANE Select	ENSP00000290866.4:n.*867_*869delinsGCA
ENST00000290866.9:c.*867_*869delinsGCA	ENSP00000290866.4:n.*867_*869delinsGCA
ENST00000428043.5:c.*1210_*1212delinsGCA	ENSP00000397593.2:n.*1210_*1212delinsGCA
ENST00000577647.2:c.1969+1248_1969+1250delinsGCA	ENSP00000464149.1:n.1969+1248_1969+1250delinsGCA
NM_000789.3:c.*867_*869delinsGCA	NP_000780.1:n.*867_*869delinsGCA
NM_001178057.1:c.*867_*869delinsGCA	NP_001171528.1:n.*867_*869delinsGCA
NM_152830.2:c.*867_*869delinsGCA	NP_690043.1:n.*867_*869delinsGCA
XM_005257110.1:c.*867_*869delinsGCA	XP_005257167.1:n.*867_*869delinsGCA
XM_006721737.2:c.*867_*869delinsGCA	XP_006721800.2:n.*867_*869delinsGCA
NM_000789.4:c.*867_*869delinsGCA MANE Select	NP_000780.1:n.*867_*869delinsGCA
NM_001178057.2:c.*867_*869delinsGCA	NP_001171528.1:n.*867_*869delinsGCA
NM_152830.3:c.*867_*869delinsGCA	NP_690043.1:n.*867_*869delinsGCA
NM_001382700.1:c.*867_*869delinsGCA	NP_001369629.1:n.*867_*869delinsGCA
NM_001382701.1:c.*867_*869delinsGCA	NP_001369630.1:n.*867_*869delinsGCA
NM_001382702.1:c.*867_*869delinsGCA	NP_001369631.1:n.*867_*869delinsGCA
NR_168483.1:n.3166_3168delinsGCA