Canonical Allele Identifier: CA2269941721

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63480900_63480901delinsGC , CM000679.2:g.63480900_63480901delinsGC	GRCh38
NC_000017.10:g.61558261_61558262delinsGC , CM000679.1:g.61558261_61558262delinsGC	GRCh37
NC_000017.9:g.58911993_58911994delinsGC	NCBI36
NG_011648.1:g.8828_8829delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.848-191_848-190delinsGC MANE Select	ENSP00000290866.4:n.848-191_848-190delinsGC
ENST00000290866.9:c.848-191_848-190delinsGC	ENSP00000290866.4:n.848-191_848-190delinsGC
ENST00000428043.5:c.848-191_848-190delinsGC	ENSP00000397593.2:n.848-191_848-190delinsGC
ENST00000582627.1:c.848-191_848-190delinsGC	ENSP00000462280.1:n.848-191_848-190delinsGC
ENST00000582678.5:c.*247-191_*247-190delinsGC	ENSP00000462995.1:n.*247-191_*247-190delinsGC
ENST00000584529.5:n.882-191_882-190delinsGC
NM_000789.3:c.848-191_848-190delinsGC	NP_000780.1:n.848-191_848-190delinsGC
XM_005257110.1:c.299-191_299-190delinsGC	XP_005257167.1:n.299-191_299-190delinsGC
NM_000789.4:c.848-191_848-190delinsGC MANE Select	NP_000780.1:n.848-191_848-190delinsGC
NM_001382700.1:c.375-191_375-190delinsGC	NP_001369629.1:n.375-191_375-190delinsGC
NM_001382701.1:c.-5-191_-5-190delinsGC	NP_001369630.1:n.-5-191_-5-190delinsGC