Canonical Allele Identifier: CA2269950675

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498337_63498339delinsCTG , CM000679.2:g.63498337_63498339delinsCTG	GRCh38
NC_000017.10:g.61575698_61575700delinsCTG , CM000679.1:g.61575698_61575700delinsCTG	GRCh37
NC_000017.9:g.58929430_58929432delinsCTG	NCBI36
NG_011648.1:g.26265_26267delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*971_*973delinsCTG MANE Select	ENSP00000290866.4:n.*971_*973delinsCTG
ENST00000290866.9:c.*971_*973delinsCTG	ENSP00000290866.4:n.*971_*973delinsCTG
ENST00000428043.5:c.*1314_*1316delinsCTG	ENSP00000397593.2:n.*1314_*1316delinsCTG
ENST00000577647.2:c.1969+1352_1969+1354delinsCTG	ENSP00000464149.1:n.1969+1352_1969+1354delinsCTG
NM_000789.3:c.*971_*973delinsCTG	NP_000780.1:n.*971_*973delinsCTG
NM_001178057.1:c.*971_*973delinsCTG	NP_001171528.1:n.*971_*973delinsCTG
NM_152830.2:c.*971_*973delinsCTG	NP_690043.1:n.*971_*973delinsCTG
XM_005257110.1:c.*971_*973delinsCTG	XP_005257167.1:n.*971_*973delinsCTG
XM_006721737.2:c.*971_*973delinsCTG	XP_006721800.2:n.*971_*973delinsCTG
NM_000789.4:c.*971_*973delinsCTG MANE Select	NP_000780.1:n.*971_*973delinsCTG
NM_001178057.2:c.*971_*973delinsCTG	NP_001171528.1:n.*971_*973delinsCTG
NM_152830.3:c.*971_*973delinsCTG	NP_690043.1:n.*971_*973delinsCTG
NM_001382700.1:c.*971_*973delinsCTG	NP_001369629.1:n.*971_*973delinsCTG
NM_001382701.1:c.*971_*973delinsCTG	NP_001369630.1:n.*971_*973delinsCTG
NM_001382702.1:c.*971_*973delinsCTG	NP_001369631.1:n.*971_*973delinsCTG
NR_168483.1:n.3270_3272delinsCTG