Canonical Allele Identifier: CA2810114488

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488554_63488555insGCTCACTGCAAGCTCCGCCTCCCG , CM000679.2:g.63488554_63488555insGCTCACTGCAAGCTCCGCCTCCCG	GRCh38
NC_000017.10:g.61565915_61565916insGCTCACTGCAAGCTCCGCCTCCCG , CM000679.1:g.61565915_61565916insGCTCACTGCAAGCTCCGCCTCCCG	GRCh37
NC_000017.9:g.58919647_58919648insGCTCACTGCAAGCTCCGCCTCCCG	NCBI36
NG_011648.1:g.16482_16483insGCTCACTGCAAGCTCCGCCTCCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCCG MANE Select	ENSP00000290866.4:n.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCC...
ENST00000290863.10:c.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000290863.6:n.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG
ENST00000290866.9:c.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000290866.4:n.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCC...
ENST00000413513.7:c.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000392247.3:n.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG
ENST00000428043.5:c.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000397593.2:n.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCC...
ENST00000577647.2:c.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000464149.1:n.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG
ENST00000578839.5:c.*376-94_*376-93insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000462110.2:n.*376-94_*376-93insGCTCACTGCAAGCTCCGCCTCCC...
ENST00000579204.1:c.487-16_487-15insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000464629.1:n.487-16_487-15insGCTCACTGCAAGCTCCGCCTCCCG
ENST00000579314.5:c.584-16_584-15insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000462599.1:n.584-16_584-15insGCTCACTGCAAGCTCCGCCTCCCG
ENST00000582005.5:c.*226-94_*226-93insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000462002.1:n.*226-94_*226-93insGCTCACTGCAAGCTCCGCCTCCC...
ENST00000582761.1:c.74-94_74-93insGCTCACTGCAAGCTCCGCCTCCCG	ENSP00000462909.1:n.74-94_74-93insGCTCACTGCAAGCTCCGCCTCCCG
ENST00000584865.5:n.252-94_252-93insGCTCACTGCAAGCTCCGCCTCCCG
NM_000789.3:c.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCCG	NP_000780.1:n.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCCG
NM_001178057.1:c.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG	NP_001171528.1:n.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG
NM_152830.2:c.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG	NP_690043.1:n.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG
XM_005257110.1:c.1757-94_1757-93insGCTCACTGCAAGCTCCGCCTCCCG	XP_005257167.1:n.1757-94_1757-93insGCTCACTGCAAGCTCCGCCTCCCG
XM_006721737.2:c.644-94_644-93insGCTCACTGCAAGCTCCGCCTCCCG	XP_006721800.2:n.644-94_644-93insGCTCACTGCAAGCTCCGCCTCCCG
XM_006721737.3:c.644-94_644-93insGCTCACTGCAAGCTCCGCCTCCCG	XP_006721800.2:n.644-94_644-93insGCTCACTGCAAGCTCCGCCTCCCG
NM_000789.4:c.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCCG MANE Select	NP_000780.1:n.2306-94_2306-93insGCTCACTGCAAGCTCCGCCTCCCG
NM_001178057.2:c.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG	NP_001171528.1:n.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG
NM_152830.3:c.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG	NP_690043.1:n.584-94_584-93insGCTCACTGCAAGCTCCGCCTCCCG
NM_001382700.1:c.1739-94_1739-93insGCTCACTGCAAGCTCCGCCTCCCG	NP_001369629.1:n.1739-94_1739-93insGCTCACTGCAAGCTCCGCCTCCCG
NM_001382701.1:c.1454-94_1454-93insGCTCACTGCAAGCTCCGCCTCCCG	NP_001369630.1:n.1454-94_1454-93insGCTCACTGCAAGCTCCGCCTCCCG
NM_001382702.1:c.236-94_236-93insGCTCACTGCAAGCTCCGCCTCCCG	NP_001369631.1:n.236-94_236-93insGCTCACTGCAAGCTCCGCCTCCCG
NR_168483.1:n.606-16_606-15insGCTCACTGCAAGCTCCGCCTCCCG