Canonical Allele Identifier: CA2269950634

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498243_63498247delinsCCTCA , CM000679.2:g.63498243_63498247delinsCCTCA	GRCh38
NC_000017.10:g.61575604_61575608delinsCCTCA , CM000679.1:g.61575604_61575608delinsCCTCA	GRCh37
NC_000017.9:g.58929336_58929340delinsCCTCA	NCBI36
NG_011648.1:g.26171_26175delinsCCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*877_*881delinsCCTCA MANE Select	ENSP00000290866.4:n.*877_*881delinsCCTCA
ENST00000290866.9:c.*877_*881delinsCCTCA	ENSP00000290866.4:n.*877_*881delinsCCTCA
ENST00000428043.5:c.*1220_*1224delinsCCTCA	ENSP00000397593.2:n.*1220_*1224delinsCCTCA
ENST00000577647.2:c.1969+1258_1969+1262delinsCCTCA	ENSP00000464149.1:n.1969+1258_1969+1262delinsCCTCA
NM_000789.3:c.*877_*881delinsCCTCA	NP_000780.1:n.*877_*881delinsCCTCA
NM_001178057.1:c.*877_*881delinsCCTCA	NP_001171528.1:n.*877_*881delinsCCTCA
NM_152830.2:c.*877_*881delinsCCTCA	NP_690043.1:n.*877_*881delinsCCTCA
XM_005257110.1:c.*877_*881delinsCCTCA	XP_005257167.1:n.*877_*881delinsCCTCA
XM_006721737.2:c.*877_*881delinsCCTCA	XP_006721800.2:n.*877_*881delinsCCTCA
NM_000789.4:c.*877_*881delinsCCTCA MANE Select	NP_000780.1:n.*877_*881delinsCCTCA
NM_001178057.2:c.*877_*881delinsCCTCA	NP_001171528.1:n.*877_*881delinsCCTCA
NM_152830.3:c.*877_*881delinsCCTCA	NP_690043.1:n.*877_*881delinsCCTCA
NM_001382700.1:c.*877_*881delinsCCTCA	NP_001369629.1:n.*877_*881delinsCCTCA
NM_001382701.1:c.*877_*881delinsCCTCA	NP_001369630.1:n.*877_*881delinsCCTCA
NM_001382702.1:c.*877_*881delinsCCTCA	NP_001369631.1:n.*877_*881delinsCCTCA
NR_168483.1:n.3176_3180delinsCCTCA