Canonical Allele Identifier: CA2269945761

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488378_63488385delinsAAAAGGAG , CM000679.2:g.63488378_63488385delinsAAAAGGAG	GRCh38
NC_000017.10:g.61565739_61565746delinsAAAAGGAG , CM000679.1:g.61565739_61565746delinsAAAAGGAG	GRCh37
NC_000017.9:g.58919471_58919478delinsAAAAGGAG	NCBI36
NG_011648.1:g.16306_16313delinsAAAAGGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2306-270_2306-263delinsAAAAGGAG MANE Select	ENSP00000290866.4:n.2306-270_2306-263delinsAAAAGGAG
ENST00000290863.10:c.584-270_584-263delinsAAAAGGAG	ENSP00000290863.6:n.584-270_584-263delinsAAAAGGAG
ENST00000290866.9:c.2306-270_2306-263delinsAAAAGGAG	ENSP00000290866.4:n.2306-270_2306-263delinsAAAAGGAG
ENST00000413513.7:c.584-270_584-263delinsAAAAGGAG	ENSP00000392247.3:n.584-270_584-263delinsAAAAGGAG
ENST00000428043.5:c.2306-270_2306-263delinsAAAAGGAG	ENSP00000397593.2:n.2306-270_2306-263delinsAAAAGGAG
ENST00000577647.2:c.584-270_584-263delinsAAAAGGAG	ENSP00000464149.1:n.584-270_584-263delinsAAAAGGAG
ENST00000578839.5:c.*376-270_*376-263delinsAAAAGGAG	ENSP00000462110.2:n.*376-270_*376-263delinsAAAAGGAG
ENST00000579204.1:c.487-192_487-185delinsAAAAGGAG	ENSP00000464629.1:n.487-192_487-185delinsAAAAGGAG
ENST00000579314.5:c.584-192_584-185delinsAAAAGGAG	ENSP00000462599.1:n.584-192_584-185delinsAAAAGGAG
ENST00000582005.5:c.*226-270_*226-263delinsAAAAGGAG	ENSP00000462002.1:n.*226-270_*226-263delinsAAAAGGAG
ENST00000582761.1:c.74-270_74-263delinsAAAAGGAG	ENSP00000462909.1:n.74-270_74-263delinsAAAAGGAG
ENST00000584865.5:n.252-270_252-263delinsAAAAGGAG
NM_000789.3:c.2306-270_2306-263delinsAAAAGGAG	NP_000780.1:n.2306-270_2306-263delinsAAAAGGAG
NM_001178057.1:c.584-270_584-263delinsAAAAGGAG	NP_001171528.1:n.584-270_584-263delinsAAAAGGAG
NM_152830.2:c.584-270_584-263delinsAAAAGGAG	NP_690043.1:n.584-270_584-263delinsAAAAGGAG
XM_005257110.1:c.1757-270_1757-263delinsAAAAGGAG	XP_005257167.1:n.1757-270_1757-263delinsAAAAGGAG
XM_006721737.2:c.644-270_644-263delinsAAAAGGAG	XP_006721800.2:n.644-270_644-263delinsAAAAGGAG
XM_006721737.3:c.644-270_644-263delinsAAAAGGAG	XP_006721800.2:n.644-270_644-263delinsAAAAGGAG
NM_000789.4:c.2306-270_2306-263delinsAAAAGGAG MANE Select	NP_000780.1:n.2306-270_2306-263delinsAAAAGGAG
NM_001178057.2:c.584-270_584-263delinsAAAAGGAG	NP_001171528.1:n.584-270_584-263delinsAAAAGGAG
NM_152830.3:c.584-270_584-263delinsAAAAGGAG	NP_690043.1:n.584-270_584-263delinsAAAAGGAG
NM_001382700.1:c.1739-270_1739-263delinsAAAAGGAG	NP_001369629.1:n.1739-270_1739-263delinsAAAAGGAG
NM_001382701.1:c.1454-270_1454-263delinsAAAAGGAG	NP_001369630.1:n.1454-270_1454-263delinsAAAAGGAG
NM_001382702.1:c.236-270_236-263delinsAAAAGGAG	NP_001369631.1:n.236-270_236-263delinsAAAAGGAG
NR_168483.1:n.606-192_606-185delinsAAAAGGAG