Canonical Allele Identifier: CA2269950618

Gene: ACE

Linked Data

• dbSNP Id: rs2030897973

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498228_63498233del , CM000679.2:g.63498228_63498233del	GRCh38
NC_000017.10:g.61575589_61575594del , CM000679.1:g.61575589_61575594del	GRCh37
NC_000017.9:g.58929321_58929326del	NCBI36
NG_011648.1:g.26156_26161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*862_*867del MANE Select	ENSP00000290866.4:n.*862_*867del
ENST00000290866.9:c.*862_*867del	ENSP00000290866.4:n.*862_*867del
ENST00000428043.5:c.*1205_*1210del	ENSP00000397593.2:n.*1205_*1210del
ENST00000577647.2:c.1969+1243_1969+1248del	ENSP00000464149.1:n.1969+1243_1969+1248del
NM_000789.3:c.*862_*867del	NP_000780.1:n.*862_*867del
NM_001178057.1:c.*862_*867del	NP_001171528.1:n.*862_*867del
NM_152830.2:c.*862_*867del	NP_690043.1:n.*862_*867del
XM_005257110.1:c.*862_*867del	XP_005257167.1:n.*862_*867del
XM_006721737.2:c.*862_*867del	XP_006721800.2:n.*862_*867del
NM_000789.4:c.*862_*867del MANE Select	NP_000780.1:n.*862_*867del
NM_001178057.2:c.*862_*867del	NP_001171528.1:n.*862_*867del
NM_152830.3:c.*862_*867del	NP_690043.1:n.*862_*867del
NM_001382700.1:c.*862_*867del	NP_001369629.1:n.*862_*867del
NM_001382701.1:c.*862_*867del	NP_001369630.1:n.*862_*867del
NM_001382702.1:c.*862_*867del	NP_001369631.1:n.*862_*867del
NR_168483.1:n.3161_3166del