Canonical Allele Identifier: CA2639237599

Gene: ACE

Linked Data

• gnomAD v4: 17-63478006-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478008del , CM000679.2:g.63478008del	GRCh38
NC_000017.10:g.61555369del , CM000679.1:g.61555369del	GRCh37
NC_000017.9:g.58909101del	NCBI36
NG_011648.1:g.5936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.327del MANE Select	ENSP00000290866.4:p.Trp109CysfsTer?
ENST00000290866.9:c.327del	ENSP00000290866.4:p.Trp109CysfsTer?
ENST00000428043.5:c.327del	ENSP00000397593.2:p.Trp109CysfsTer?
ENST00000579462.1:n.352del
ENST00000580318.1:n.516del
ENST00000582627.1:c.327del	ENSP00000462280.1:p.Trp109CysfsTer?
ENST00000582678.5:c.327del	ENSP00000462995.1:p.Trp109CysfsTer?
ENST00000583336.5:n.361del
ENST00000584529.5:n.361del
NM_000789.3:c.327del	NP_000780.1:p.Trp109CysfsTer?
XM_005257110.1:c.-129del	XP_005257167.1:n.-129del
NM_000789.4:c.327del MANE Select	NP_000780.1:p.Trp109CysfsTer?
NM_001382700.1:c.92del	NP_001369629.1:p.Gly31AlafsTer27
NM_001382701.1:c.-288del	NP_001369630.1:n.-288del