Canonical Allele Identifier: CA15909792

Gene: ACE

Linked Data

• dbSNP Id: rs4329
• gnomAD v2: 17-61563458-A-G
• gnomAD v3: 17-63486097-A-G
• gnomAD v4: 17-63486097-A-G
• MyVariant Identifiers: chr17:g.61563458A>G (hg19) ; chr17:g.63486097A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486097A>G , CM000679.2:g.63486097A>G	GRCh38
NC_000017.10:g.61563458A>G , CM000679.1:g.61563458A>G	GRCh37
NC_000017.9:g.58917190A>G	NCBI36
NG_011648.1:g.14025A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2059-460A>G MANE Select	ENSP00000290866.4:n.2059-460A>G
ENST00000290863.10:c.337-460A>G	ENSP00000290863.6:n.337-460A>G
ENST00000290866.9:c.2059-460A>G	ENSP00000290866.4:n.2059-460A>G
ENST00000413513.7:c.337-460A>G	ENSP00000392247.3:n.337-460A>G
ENST00000428043.5:c.2059-460A>G	ENSP00000397593.2:n.2059-460A>G
ENST00000577647.2:c.337-460A>G	ENSP00000464149.1:n.337-460A>G
ENST00000578839.5:c.*129-460A>G	ENSP00000462110.2:n.*129-460A>G
ENST00000579204.1:c.240-460A>G	ENSP00000464629.1:n.240-460A>G
ENST00000579314.5:c.337-460A>G	ENSP00000462599.1:n.337-460A>G
ENST00000579726.5:c.608-262A>G
ENST00000582005.5:c.337-195A>G	ENSP00000462002.1:n.337-195A>G
NM_000789.3:c.2059-460A>G	NP_000780.1:n.2059-460A>G
NM_001178057.1:c.337-460A>G	NP_001171528.1:n.337-460A>G
NM_152830.2:c.337-460A>G	NP_690043.1:n.337-460A>G
XM_005257110.1:c.1510-460A>G	XP_005257167.1:n.1510-460A>G
XM_006721737.2:c.397-460A>G	XP_006721800.2:n.397-460A>G
XM_006721737.3:c.397-460A>G	XP_006721800.2:n.397-460A>G
NM_000789.4:c.2059-460A>G MANE Select	NP_000780.1:n.2059-460A>G
NM_001178057.2:c.337-460A>G	NP_001171528.1:n.337-460A>G
NM_152830.3:c.337-460A>G	NP_690043.1:n.337-460A>G
NM_001382700.1:c.1492-460A>G	NP_001369629.1:n.1492-460A>G
NM_001382701.1:c.1207-460A>G	NP_001369630.1:n.1207-460A>G
NM_001382702.1:c.-12-460A>G	NP_001369631.1:n.-12-460A>G
NR_168483.1:n.359-460A>G