Canonical Allele Identifier: CA2639237105

Gene: ACE

Linked Data

• gnomAD v4: 17-63477265-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477266del , CM000679.2:g.63477266del	GRCh38
NC_000017.10:g.61554627del , CM000679.1:g.61554627del	GRCh37
NC_000017.9:g.58908359del	NCBI36
NG_011648.1:g.5194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.172del MANE Select	ENSP00000290866.4:p.Glu58AsnfsTer?
ENST00000290866.9:c.172del	ENSP00000290866.4:p.Glu58AsnfsTer?
ENST00000428043.5:c.172del	ENSP00000397593.2:p.Glu58AsnfsTer?
ENST00000579462.1:n.197del
ENST00000582678.5:c.172del	ENSP00000462995.1:p.Glu58AsnfsTer?
ENST00000583336.5:n.206del
ENST00000584529.5:n.206del
NM_000789.3:c.172del	NP_000780.1:p.Glu58AsnfsTer?
XM_005257110.1:c.-284del	XP_005257167.1:n.-284del
NM_000789.4:c.172del MANE Select	NP_000780.1:p.Glu58AsnfsTer?
NM_001382700.1:c.-64del	NP_001369629.1:n.-64del
NM_001382701.1:c.-443del	NP_001369630.1:n.-443del