Canonical Allele Identifier: CA2269946116

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63489016_63489017delinsTC , CM000679.2:g.63489016_63489017delinsTC	GRCh38
NC_000017.10:g.61566377_61566378delinsTC , CM000679.1:g.61566377_61566378delinsTC	GRCh37
NC_000017.9:g.58920109_58920110delinsTC	NCBI36
NG_011648.1:g.16944_16945delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2525_2526delinsTC MANE Select	ENSP00000290866.4:p.Phe842=
ENST00000290863.10:c.803_804delinsTC	ENSP00000290863.6:p.Phe268=
ENST00000290866.9:c.2525_2526delinsTC	ENSP00000290866.4:p.Phe842=
ENST00000413513.7:c.803_804delinsTC	ENSP00000392247.3:p.Phe268=
ENST00000428043.5:c.2525_2526delinsTC	ENSP00000397593.2:p.Phe842=
ENST00000577647.2:c.803_804delinsTC	ENSP00000464149.1:p.Phe268=
ENST00000578839.5:c.*519+225_*519+226delinsTC	ENSP00000462110.2:n.*519+225_*519+226delinsTC
ENST00000579204.1:c.784_785delinsTC	ENSP00000464629.1:n.784_785delinsTC
ENST00000579314.5:c.*254_*255delinsTC	ENSP00000462599.1:n.*254_*255delinsTC
ENST00000582005.5:c.*445_*446delinsTC	ENSP00000462002.1:n.*445_*446delinsTC
ENST00000582761.1:c.293_294delinsTC	ENSP00000462909.1:p.Phe98=
ENST00000584865.5:n.471_472delinsTC
NM_000789.3:c.2525_2526delinsTC	NP_000780.1:p.Phe842=
NM_001178057.1:c.803_804delinsTC	NP_001171528.1:p.Phe268=
NM_152830.2:c.803_804delinsTC	NP_690043.1:p.Phe268=
XM_005257110.1:c.1976_1977delinsTC	XP_005257167.1:p.Phe659=
XM_006721737.2:c.863_864delinsTC	XP_006721800.2:p.Phe288=
XM_006721737.3:c.863_864delinsTC	XP_006721800.2:p.Phe288=
NM_000789.4:c.2525_2526delinsTC MANE Select	NP_000780.1:p.Phe842=
NM_001178057.2:c.803_804delinsTC	NP_001171528.1:p.Phe268=
NM_152830.3:c.803_804delinsTC	NP_690043.1:p.Phe268=
NM_001382700.1:c.1958_1959delinsTC	NP_001369629.1:p.Phe653=
NM_001382701.1:c.1673_1674delinsTC	NP_001369630.1:p.Phe558=
NM_001382702.1:c.379+225_379+226delinsTC	NP_001369631.1:n.379+225_379+226delinsTC
NR_168483.1:n.903_904delinsTC