Canonical Allele Identifier: CA627148141

Gene: ACE

Linked Data

• dbSNP Id: rs1599148509
• gnomAD v2: 17-61565907-G-GTCGCCCAGGC
• gnomAD v3: 17-63488546-G-GTCGCCCAGGC
• gnomAD v4: 17-63488546-G-GTCGCCCAGGC
• MyVariant Identifiers: chr17:g.61565907_61565908insTCGCCCAGGC (hg19) ; chr17:g.63488546_63488547insTCGCCCAGGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488547_63488548insCGCCCAGGCT , CM000679.2:g.63488547_63488548insCGCCCAGGCT	GRCh38
NC_000017.10:g.61565908_61565909insCGCCCAGGCT , CM000679.1:g.61565908_61565909insCGCCCAGGCT	GRCh37
NC_000017.9:g.58919640_58919641insCGCCCAGGCT	NCBI36
NG_011648.1:g.16475_16476insCGCCCAGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2306-101_2306-100insCGCCCAGGCT MANE Select	ENSP00000290866.4:n.2306-101_2306-100insCGCCCAGGCT
ENST00000290863.10:c.584-101_584-100insCGCCCAGGCT	ENSP00000290863.6:n.584-101_584-100insCGCCCAGGCT
ENST00000290866.9:c.2306-101_2306-100insCGCCCAGGCT	ENSP00000290866.4:n.2306-101_2306-100insCGCCCAGGCT
ENST00000413513.7:c.584-101_584-100insCGCCCAGGCT	ENSP00000392247.3:n.584-101_584-100insCGCCCAGGCT
ENST00000428043.5:c.2306-101_2306-100insCGCCCAGGCT	ENSP00000397593.2:n.2306-101_2306-100insCGCCCAGGCT
ENST00000577647.2:c.584-101_584-100insCGCCCAGGCT	ENSP00000464149.1:n.584-101_584-100insCGCCCAGGCT
ENST00000578839.5:c.*376-101_*376-100insCGCCCAGGCT	ENSP00000462110.2:n.*376-101_*376-100insCGCCCAGGCT
ENST00000579204.1:c.487-23_487-22insCGCCCAGGCT	ENSP00000464629.1:n.487-23_487-22insCGCCCAGGCT
ENST00000579314.5:c.584-23_584-22insCGCCCAGGCT	ENSP00000462599.1:n.584-23_584-22insCGCCCAGGCT
ENST00000582005.5:c.*226-101_*226-100insCGCCCAGGCT	ENSP00000462002.1:n.*226-101_*226-100insCGCCCAGGCT
ENST00000582761.1:c.74-101_74-100insCGCCCAGGCT	ENSP00000462909.1:n.74-101_74-100insCGCCCAGGCT
ENST00000584865.5:n.252-101_252-100insCGCCCAGGCT
NM_000789.3:c.2306-101_2306-100insCGCCCAGGCT	NP_000780.1:n.2306-101_2306-100insCGCCCAGGCT
NM_001178057.1:c.584-101_584-100insCGCCCAGGCT	NP_001171528.1:n.584-101_584-100insCGCCCAGGCT
NM_152830.2:c.584-101_584-100insCGCCCAGGCT	NP_690043.1:n.584-101_584-100insCGCCCAGGCT
XM_005257110.1:c.1757-101_1757-100insCGCCCAGGCT	XP_005257167.1:n.1757-101_1757-100insCGCCCAGGCT
XM_006721737.2:c.644-101_644-100insCGCCCAGGCT	XP_006721800.2:n.644-101_644-100insCGCCCAGGCT
XM_006721737.3:c.644-101_644-100insCGCCCAGGCT	XP_006721800.2:n.644-101_644-100insCGCCCAGGCT
NM_000789.4:c.2306-101_2306-100insCGCCCAGGCT MANE Select	NP_000780.1:n.2306-101_2306-100insCGCCCAGGCT
NM_001178057.2:c.584-101_584-100insCGCCCAGGCT	NP_001171528.1:n.584-101_584-100insCGCCCAGGCT
NM_152830.3:c.584-101_584-100insCGCCCAGGCT	NP_690043.1:n.584-101_584-100insCGCCCAGGCT
NM_001382700.1:c.1739-101_1739-100insCGCCCAGGCT	NP_001369629.1:n.1739-101_1739-100insCGCCCAGGCT
NM_001382701.1:c.1454-101_1454-100insCGCCCAGGCT	NP_001369630.1:n.1454-101_1454-100insCGCCCAGGCT
NM_001382702.1:c.236-101_236-100insCGCCCAGGCT	NP_001369631.1:n.236-101_236-100insCGCCCAGGCT
NR_168483.1:n.606-23_606-22insCGCCCAGGCT