Canonical Allele Identifier: CA773972278

Gene: ACE

Linked Data

• dbSNP Id: rs1320806017
• MyVariant Identifiers: chr17:g.61572421_61572422insC (hg19) ; chr17:g.63495060_63495061insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63495060_63495061insC , CM000679.2:g.63495060_63495061insC	GRCh38
NC_000017.10:g.61572421_61572422insC , CM000679.1:g.61572421_61572422insC	GRCh37
NC_000017.9:g.58926153_58926154insC	NCBI36
NG_011648.1:g.22988_22989insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3380+590_3380+591insC MANE Select	ENSP00000290866.4:n.3380+590_3380+591insC
ENST00000290863.10:c.1658+590_1658+591insC	ENSP00000290863.6:n.1658+590_1658+591insC
ENST00000290866.9:c.3380+590_3380+591insC	ENSP00000290866.4:n.3380+590_3380+591insC
ENST00000413513.7:c.1658+590_1658+591insC	ENSP00000392247.3:n.1658+590_1658+591insC
ENST00000428043.5:c.3380+590_3380+591insC	ENSP00000397593.2:n.3380+590_3380+591insC
ENST00000577418.5:n.390+590_390+591insC
ENST00000577647.2:c.1658+590_1658+591insC	ENSP00000464149.1:n.1658+590_1658+591insC
ENST00000578839.5:c.*1258+590_*1258+591insC	ENSP00000462110.2:n.*1258+590_*1258+591insC
ENST00000579314.5:c.*1109+590_*1109+591insC	ENSP00000462599.1:n.*1109+590_*1109+591insC
ENST00000579409.1:c.67+590_67+591insC
NM_000789.3:c.3380+590_3380+591insC	NP_000780.1:n.3380+590_3380+591insC
NM_001178057.1:c.1658+590_1658+591insC	NP_001171528.1:n.1658+590_1658+591insC
NM_152830.2:c.1658+590_1658+591insC	NP_690043.1:n.1658+590_1658+591insC
XM_005257110.1:c.2831+590_2831+591insC	XP_005257167.1:n.2831+590_2831+591insC
XM_006721737.2:c.1718+590_1718+591insC	XP_006721800.2:n.1718+590_1718+591insC
XM_006721737.3:c.1718+590_1718+591insC	XP_006721800.2:n.1718+590_1718+591insC
NM_000789.4:c.3380+590_3380+591insC MANE Select	NP_000780.1:n.3380+590_3380+591insC
NM_001178057.2:c.1658+590_1658+591insC	NP_001171528.1:n.1658+590_1658+591insC
NM_152830.3:c.1658+590_1658+591insC	NP_690043.1:n.1658+590_1658+591insC
NM_001382700.1:c.2813+590_2813+591insC	NP_001369629.1:n.2813+590_2813+591insC
NM_001382701.1:c.2528+590_2528+591insC	NP_001369630.1:n.2528+590_2528+591insC
NM_001382702.1:c.1118+590_1118+591insC	NP_001369631.1:n.1118+590_1118+591insC
NR_168483.1:n.1758+590_1758+591insC