Canonical Allele Identifier: CA2639237598

Gene: ACE

Linked Data

• gnomAD v4: 17-63477944-TGCTCAGCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477946_63477954del , CM000679.2:g.63477946_63477954del	GRCh38
NC_000017.10:g.61555307_61555315del , CM000679.1:g.61555307_61555315del	GRCh37
NC_000017.9:g.58909039_58909047del	NCBI36
NG_011648.1:g.5874_5882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.265_273del MANE Select	ENSP00000290866.4:p.Leu89_Gln91del
ENST00000290866.9:c.265_273del	ENSP00000290866.4:p.Leu89_Gln91del
ENST00000428043.5:c.265_273del	ENSP00000397593.2:p.Leu89_Gln91del
ENST00000579462.1:n.290_298del
ENST00000580318.1:n.454_462del
ENST00000582627.1:c.265_273del	ENSP00000462280.1:p.Leu89_Gln91del
ENST00000582678.5:c.265_273del	ENSP00000462995.1:p.Leu89_Gln91del
ENST00000583336.5:n.299_307del
ENST00000584529.5:n.299_307del
NM_000789.3:c.265_273del	NP_000780.1:p.Leu89_Gln91del
XM_005257110.1:c.-191_-183del	XP_005257167.1:n.-191_-183del
NM_000789.4:c.265_273del MANE Select	NP_000780.1:p.Leu89_Gln91del
NM_001382700.1:c.30_38del	NP_001369629.1:p.Cys10_Arg13delinsTrp
NM_001382701.1:c.-350_-342del	NP_001369630.1:n.-350_-342del