Canonical Allele Identifier: CA2269950674

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498335_63498339delinsAACTG , CM000679.2:g.63498335_63498339delinsAACTG	GRCh38
NC_000017.10:g.61575696_61575700delinsAACTG , CM000679.1:g.61575696_61575700delinsAACTG	GRCh37
NC_000017.9:g.58929428_58929432delinsAACTG	NCBI36
NG_011648.1:g.26263_26267delinsAACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*969_*973delinsAACTG MANE Select	ENSP00000290866.4:n.*969_*973delinsAACTG
ENST00000290866.9:c.*969_*973delinsAACTG	ENSP00000290866.4:n.*969_*973delinsAACTG
ENST00000428043.5:c.*1312_*1316delinsAACTG	ENSP00000397593.2:n.*1312_*1316delinsAACTG
ENST00000577647.2:c.1969+1350_1969+1354delinsAACTG	ENSP00000464149.1:n.1969+1350_1969+1354delinsAACTG
NM_000789.3:c.*969_*973delinsAACTG	NP_000780.1:n.*969_*973delinsAACTG
NM_001178057.1:c.*969_*973delinsAACTG	NP_001171528.1:n.*969_*973delinsAACTG
NM_152830.2:c.*969_*973delinsAACTG	NP_690043.1:n.*969_*973delinsAACTG
XM_005257110.1:c.*969_*973delinsAACTG	XP_005257167.1:n.*969_*973delinsAACTG
XM_006721737.2:c.*969_*973delinsAACTG	XP_006721800.2:n.*969_*973delinsAACTG
NM_000789.4:c.*969_*973delinsAACTG MANE Select	NP_000780.1:n.*969_*973delinsAACTG
NM_001178057.2:c.*969_*973delinsAACTG	NP_001171528.1:n.*969_*973delinsAACTG
NM_152830.3:c.*969_*973delinsAACTG	NP_690043.1:n.*969_*973delinsAACTG
NM_001382700.1:c.*969_*973delinsAACTG	NP_001369629.1:n.*969_*973delinsAACTG
NM_001382701.1:c.*969_*973delinsAACTG	NP_001369630.1:n.*969_*973delinsAACTG
NM_001382702.1:c.*969_*973delinsAACTG	NP_001369631.1:n.*969_*973delinsAACTG
NR_168483.1:n.3268_3272delinsAACTG