Canonical Allele Identifier: CA292870249

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477132_63477137del , CM000679.2:g.63477132_63477137del	GRCh38
NC_000017.10:g.61554493_61554498del , CM000679.1:g.61554493_61554498del	GRCh37
NC_000017.9:g.58908225_58908230del	NCBI36
NG_011648.1:g.5060_5065del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.38_43del MANE Select	ENSP00000290866.4:p.Leu13_Leu14del
ENST00000290866.9:c.38_43del	ENSP00000290866.4:p.Leu13_Leu14del
ENST00000428043.5:c.38_43del	ENSP00000397593.2:p.Leu13_Leu14del
ENST00000579462.1:n.63_68del
ENST00000582678.5:c.38_43del	ENSP00000462995.1:p.Leu13_Leu14del
ENST00000583336.5:n.72_77del
ENST00000584529.5:n.72_77del
NM_000789.3:c.38_43del	NP_000780.1:p.Leu13_Leu14del
XM_005257110.1:c.-418_-413del	XP_005257167.1:n.-418_-413del
NM_000789.4:c.38_43del MANE Select	NP_000780.1:p.Leu13_Leu14del
NM_001382700.1:c.-198_-193del	NP_001369629.1:n.-198_-193del
NM_001382701.1:c.-577_-572del	NP_001369630.1:n.-577_-572del