Canonical Allele Identifier: CA292889324

Gene: ACE

Linked Data

• dbSNP Id: rs532952262
• gnomAD v3: 17-63495002-T-G
• gnomAD v4: 17-63495002-T-G
• MyVariant Identifiers: chr17:g.61572363T>G (hg19) ; chr17:g.63495002T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63495002T>G , CM000679.2:g.63495002T>G	GRCh38
NC_000017.10:g.61572363T>G , CM000679.1:g.61572363T>G	GRCh37
NC_000017.9:g.58926095T>G	NCBI36
NG_011648.1:g.22930T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3380+532T>G MANE Select	ENSP00000290866.4:n.3380+532T>G
ENST00000290863.10:c.1658+532T>G	ENSP00000290863.6:n.1658+532T>G
ENST00000290866.9:c.3380+532T>G	ENSP00000290866.4:n.3380+532T>G
ENST00000413513.7:c.1658+532T>G	ENSP00000392247.3:n.1658+532T>G
ENST00000428043.5:c.3380+532T>G	ENSP00000397593.2:n.3380+532T>G
ENST00000577418.5:n.390+532T>G
ENST00000577647.2:c.1658+532T>G	ENSP00000464149.1:n.1658+532T>G
ENST00000578839.5:c.*1258+532T>G	ENSP00000462110.2:n.*1258+532T>G
ENST00000579314.5:c.*1109+532T>G	ENSP00000462599.1:n.*1109+532T>G
ENST00000579409.1:c.67+532T>G
NM_000789.3:c.3380+532T>G	NP_000780.1:n.3380+532T>G
NM_001178057.1:c.1658+532T>G	NP_001171528.1:n.1658+532T>G
NM_152830.2:c.1658+532T>G	NP_690043.1:n.1658+532T>G
XM_005257110.1:c.2831+532T>G	XP_005257167.1:n.2831+532T>G
XM_006721737.2:c.1718+532T>G	XP_006721800.2:n.1718+532T>G
XM_006721737.3:c.1718+532T>G	XP_006721800.2:n.1718+532T>G
NM_000789.4:c.3380+532T>G MANE Select	NP_000780.1:n.3380+532T>G
NM_001178057.2:c.1658+532T>G	NP_001171528.1:n.1658+532T>G
NM_152830.3:c.1658+532T>G	NP_690043.1:n.1658+532T>G
NM_001382700.1:c.2813+532T>G	NP_001369629.1:n.2813+532T>G
NM_001382701.1:c.2528+532T>G	NP_001369630.1:n.2528+532T>G
NM_001382702.1:c.1118+532T>G	NP_001369631.1:n.1118+532T>G
NR_168483.1:n.1758+532T>G