Canonical Allele Identifier: CA2639237592

Gene: ACE

Linked Data

• gnomAD v4: 17-63477920-GTGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477921_63477923del , CM000679.2:g.63477921_63477923del	GRCh38
NC_000017.10:g.61555282_61555284del , CM000679.1:g.61555282_61555284del	GRCh37
NC_000017.9:g.58909014_58909016del	NCBI36
NG_011648.1:g.5849_5851del

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.250-10_250-8del MANE Select	ENSP00000290866.4:n.250-10_250-8del
ENST00000290866.9:c.250-10_250-8del	ENSP00000290866.4:n.250-10_250-8del
ENST00000428043.5:c.250-10_250-8del	ENSP00000397593.2:n.250-10_250-8del
ENST00000579462.1:n.275-10_275-8del
ENST00000580318.1:n.429_431del
ENST00000582627.1:c.250-10_250-8del	ENSP00000462280.1:n.250-10_250-8del
ENST00000582678.5:c.250-10_250-8del	ENSP00000462995.1:n.250-10_250-8del
ENST00000583336.5:n.284-10_284-8del
ENST00000584529.5:n.284-10_284-8del
NM_000789.3:c.250-10_250-8del	NP_000780.1:n.250-10_250-8del
XM_005257110.1:c.-206-10_-206-8del	XP_005257167.1:n.-206-10_-206-8del
NM_000789.4:c.250-10_250-8del MANE Select	NP_000780.1:n.250-10_250-8del
NM_001382700.1:c.15-10_15-8del	NP_001369629.1:n.15-10_15-8del
NM_001382701.1:c.-365-10_-365-8del	NP_001369630.1:n.-365-10_-365-8del