Canonical Allele Identifier: CA2269950677

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498341_63498344delinsAAAG , CM000679.2:g.63498341_63498344delinsAAAG	GRCh38
NC_000017.10:g.61575702_61575705delinsAAAG , CM000679.1:g.61575702_61575705delinsAAAG	GRCh37
NC_000017.9:g.58929434_58929437delinsAAAG	NCBI36
NG_011648.1:g.26269_26272delinsAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*975_*978delinsAAAG MANE Select	ENSP00000290866.4:n.*975_*978delinsAAAG
ENST00000290866.9:c.*975_*978delinsAAAG	ENSP00000290866.4:n.*975_*978delinsAAAG
ENST00000428043.5:c.*1318_*1321delinsAAAG	ENSP00000397593.2:n.*1318_*1321delinsAAAG
ENST00000577647.2:c.1969+1356_1969+1359delinsAAAG	ENSP00000464149.1:n.1969+1356_1969+1359delinsAAAG
NM_000789.3:c.*975_*978delinsAAAG	NP_000780.1:n.*975_*978delinsAAAG
NM_001178057.1:c.*975_*978delinsAAAG	NP_001171528.1:n.*975_*978delinsAAAG
NM_152830.2:c.*975_*978delinsAAAG	NP_690043.1:n.*975_*978delinsAAAG
XM_005257110.1:c.*975_*978delinsAAAG	XP_005257167.1:n.*975_*978delinsAAAG
XM_006721737.2:c.*975_*978delinsAAAG	XP_006721800.2:n.*975_*978delinsAAAG
NM_000789.4:c.*975_*978delinsAAAG MANE Select	NP_000780.1:n.*975_*978delinsAAAG
NM_001178057.2:c.*975_*978delinsAAAG	NP_001171528.1:n.*975_*978delinsAAAG
NM_152830.3:c.*975_*978delinsAAAG	NP_690043.1:n.*975_*978delinsAAAG
NM_001382700.1:c.*975_*978delinsAAAG	NP_001369629.1:n.*975_*978delinsAAAG
NM_001382701.1:c.*975_*978delinsAAAG	NP_001369630.1:n.*975_*978delinsAAAG
NM_001382702.1:c.*975_*978delinsAAAG	NP_001369631.1:n.*975_*978delinsAAAG
NR_168483.1:n.3274_3277delinsAAAG