Canonical Allele Identifier: CA2639237556

Gene: ACE

Linked Data

• gnomAD v4: 17-63477869-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477870_63477871del , CM000679.2:g.63477870_63477871del	GRCh38
NC_000017.10:g.61555231_61555232del , CM000679.1:g.61555231_61555232del	GRCh37
NC_000017.9:g.58908963_58908964del	NCBI36
NG_011648.1:g.5798_5799del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.250-61_250-60del MANE Select	ENSP00000290866.4:n.250-61_250-60del
ENST00000290866.9:c.250-61_250-60del	ENSP00000290866.4:n.250-61_250-60del
ENST00000428043.5:c.250-61_250-60del	ENSP00000397593.2:n.250-61_250-60del
ENST00000579462.1:n.275-61_275-60del
ENST00000580318.1:n.378_379del
ENST00000582627.1:c.250-61_250-60del	ENSP00000462280.1:n.250-61_250-60del
ENST00000582678.5:c.250-61_250-60del	ENSP00000462995.1:n.250-61_250-60del
ENST00000583336.5:n.284-61_284-60del
ENST00000584529.5:n.284-61_284-60del
NM_000789.3:c.250-61_250-60del	NP_000780.1:n.250-61_250-60del
XM_005257110.1:c.-206-61_-206-60del	XP_005257167.1:n.-206-61_-206-60del
NM_000789.4:c.250-61_250-60del MANE Select	NP_000780.1:n.250-61_250-60del
NM_001382700.1:c.15-61_15-60del	NP_001369629.1:n.15-61_15-60del
NM_001382701.1:c.-365-61_-365-60del	NP_001369630.1:n.-365-61_-365-60del