Canonical Allele Identifier: CA8699098

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63479123_63479136del , CM000679.2:g.63479123_63479136del	GRCh38
NC_000017.10:g.61556484_61556497del , CM000679.1:g.61556484_61556497del	GRCh37
NC_000017.9:g.58910216_58910229del	NCBI36
NG_011648.1:g.7051_7064del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.511+23_511+36del MANE Select	ENSP00000290866.4:n.511+23_511+36del
ENST00000290866.9:c.511+23_511+36del	ENSP00000290866.4:n.511+23_511+36del
ENST00000428043.5:c.511+23_511+36del	ENSP00000397593.2:n.511+23_511+36del
ENST00000580318.1:n.700+23_700+36del
ENST00000582627.1:c.511+23_511+36del	ENSP00000462280.1:n.511+23_511+36del
ENST00000582678.5:c.418-646_418-633del	ENSP00000462995.1:n.418-646_418-633del
ENST00000584529.5:n.545+23_545+36del
NM_000789.3:c.511+23_511+36del	NP_000780.1:n.511+23_511+36del
XM_005257110.1:c.-38-646_-38-633del	XP_005257167.1:n.-38-646_-38-633del
NM_000789.4:c.511+23_511+36del MANE Select	NP_000780.1:n.511+23_511+36del
NM_001382700.1:c.182+1025_182+1038del	NP_001369629.1:n.182+1025_182+1038del
NM_001382701.1:c.-198+1025_-198+1038del	NP_001369630.1:n.-198+1025_-198+1038del