Canonical Allele Identifier: CA627148155

Gene: ACE

Linked Data

• dbSNP Id: rs1341950338
• gnomAD v2: 17-61565911-T-TGGCGGGATCTCGGCTCACTGCAAGC
• MyVariant Identifiers: chr17:g.61565911_61565912insGGCGGGATCTCGGCTCACTGCAAGC (hg19) ; chr17:g.63488550_63488551insGGCGGGATCTCGGCTCACTGCAAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488550_63488551insGGCGGGATCTCGGCTCACTGCAAGC , CM000679.2:g.63488550_63488551insGGCGGGATCTCGGCTCACTGCAAGC	GRCh38
NC_000017.10:g.61565911_61565912insGGCGGGATCTCGGCTCACTGCAAGC , CM000679.1:g.61565911_61565912insGGCGGGATCTCGGCTCACTGCAAGC	GRCh37
NC_000017.9:g.58919643_58919644insGGCGGGATCTCGGCTCACTGCAAGC	NCBI36
NG_011648.1:g.16478_16479insGGCGGGATCTCGGCTCACTGCAAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAAGC MANE Select	ENSP00000290866.4:n.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAA...
ENST00000290863.10:c.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000290863.6:n.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC...
ENST00000290866.9:c.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000290866.4:n.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAA...
ENST00000413513.7:c.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000392247.3:n.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC...
ENST00000428043.5:c.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000397593.2:n.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAA...
ENST00000577647.2:c.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000464149.1:n.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC...
ENST00000578839.5:c.*376-98_*376-97insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000462110.2:n.*376-98_*376-97insGGCGGGATCTCGGCTCACTGCAA...
ENST00000579204.1:c.487-20_487-19insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000464629.1:n.487-20_487-19insGGCGGGATCTCGGCTCACTGCAAGC...
ENST00000579314.5:c.584-20_584-19insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000462599.1:n.584-20_584-19insGGCGGGATCTCGGCTCACTGCAAGC...
ENST00000582005.5:c.*226-98_*226-97insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000462002.1:n.*226-98_*226-97insGGCGGGATCTCGGCTCACTGCAA...
ENST00000582761.1:c.74-98_74-97insGGCGGGATCTCGGCTCACTGCAAGC	ENSP00000462909.1:n.74-98_74-97insGGCGGGATCTCGGCTCACTGCAAGC
ENST00000584865.5:n.252-98_252-97insGGCGGGATCTCGGCTCACTGCAAGC
NM_000789.3:c.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAAGC	NP_000780.1:n.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAAGC
NM_001178057.1:c.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC	NP_001171528.1:n.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC
NM_152830.2:c.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC	NP_690043.1:n.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC
XM_005257110.1:c.1757-98_1757-97insGGCGGGATCTCGGCTCACTGCAAGC	XP_005257167.1:n.1757-98_1757-97insGGCGGGATCTCGGCTCACTGCAAGC
XM_006721737.2:c.644-98_644-97insGGCGGGATCTCGGCTCACTGCAAGC	XP_006721800.2:n.644-98_644-97insGGCGGGATCTCGGCTCACTGCAAGC
XM_006721737.3:c.644-98_644-97insGGCGGGATCTCGGCTCACTGCAAGC	XP_006721800.2:n.644-98_644-97insGGCGGGATCTCGGCTCACTGCAAGC
NM_000789.4:c.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAAGC MANE Select	NP_000780.1:n.2306-98_2306-97insGGCGGGATCTCGGCTCACTGCAAGC
NM_001178057.2:c.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC	NP_001171528.1:n.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC
NM_152830.3:c.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC	NP_690043.1:n.584-98_584-97insGGCGGGATCTCGGCTCACTGCAAGC
NM_001382700.1:c.1739-98_1739-97insGGCGGGATCTCGGCTCACTGCAAGC	NP_001369629.1:n.1739-98_1739-97insGGCGGGATCTCGGCTCACTGCAAGC
NM_001382701.1:c.1454-98_1454-97insGGCGGGATCTCGGCTCACTGCAAGC	NP_001369630.1:n.1454-98_1454-97insGGCGGGATCTCGGCTCACTGCAAGC
NM_001382702.1:c.236-98_236-97insGGCGGGATCTCGGCTCACTGCAAGC	NP_001369631.1:n.236-98_236-97insGGCGGGATCTCGGCTCACTGCAAGC
NR_168483.1:n.606-20_606-19insGGCGGGATCTCGGCTCACTGCAAGC