Canonical Allele Identifier: CA2269942602

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482482_63482483delinsCG , CM000679.2:g.63482482_63482483delinsCG	GRCh38
NC_000017.10:g.61559843_61559844delinsCG , CM000679.1:g.61559843_61559844delinsCG	GRCh37
NC_000017.9:g.58913575_58913576delinsCG	NCBI36
NG_011648.1:g.10410_10411delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1135_1136delinsCG MANE Select	ENSP00000290866.4:p.Arg379=
ENST00000290866.9:c.1135_1136delinsCG	ENSP00000290866.4:p.Arg379=
ENST00000428043.5:c.1135_1136delinsCG	ENSP00000397593.2:p.Arg379=
ENST00000582678.5:c.*534_*535delinsCG	ENSP00000462995.1:n.*534_*535delinsCG
ENST00000584529.5:n.1169_1170delinsCG
NM_000789.3:c.1135_1136delinsCG	NP_000780.1:p.Arg379=
XM_005257110.1:c.586_587delinsCG	XP_005257167.1:p.Arg196=
NM_000789.4:c.1135_1136delinsCG MANE Select	NP_000780.1:p.Arg379=
NM_001382700.1:c.568_569delinsCG	NP_001369629.1:p.Arg190=
NM_001382701.1:c.283_284delinsCG	NP_001369630.1:p.Arg95=