Canonical Allele Identifier: CA2269940087

Gene: ACE

Linked Data

• dbSNP Id: rs2049641156

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477689_63477695del , CM000679.2:g.63477689_63477695del	GRCh38
NC_000017.10:g.61555050_61555056del , CM000679.1:g.61555050_61555056del	GRCh37
NC_000017.9:g.58908782_58908788del	NCBI36
NG_011648.1:g.5617_5623del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.250-242_250-236del MANE Select	ENSP00000290866.4:n.250-242_250-236del
ENST00000290866.9:c.250-242_250-236del	ENSP00000290866.4:n.250-242_250-236del
ENST00000428043.5:c.250-242_250-236del	ENSP00000397593.2:n.250-242_250-236del
ENST00000579462.1:n.275-242_275-236del
ENST00000580318.1:n.197_203del
ENST00000582627.1:c.148_154del	ENSP00000462280.1:p.Pro50SerfsTer?
ENST00000582678.5:c.250-242_250-236del	ENSP00000462995.1:n.250-242_250-236del
ENST00000583336.5:n.284-242_284-236del
ENST00000584529.5:n.284-242_284-236del
NM_000789.3:c.250-242_250-236del	NP_000780.1:n.250-242_250-236del
XM_005257110.1:c.-206-242_-206-236del	XP_005257167.1:n.-206-242_-206-236del
NM_000789.4:c.250-242_250-236del MANE Select	NP_000780.1:n.250-242_250-236del
NM_001382700.1:c.15-242_15-236del	NP_001369629.1:n.15-242_15-236del
NM_001382701.1:c.-365-242_-365-236del	NP_001369630.1:n.-365-242_-365-236del