Canonical Allele Identifier: CA626842085

Gene: ACE

Linked Data

• dbSNP Id: rs1176163569
• gnomAD v2: 17-61560771-A-G
• gnomAD v4: 17-63483410-A-G
• MyVariant Identifiers: chr17:g.61560771A>G (hg19) ; chr17:g.63483410A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63483410A>G , CM000679.2:g.63483410A>G	GRCh38
NC_000017.10:g.61560771A>G , CM000679.1:g.61560771A>G	GRCh37
NC_000017.9:g.58914503A>G	NCBI36
NG_011648.1:g.11338A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1488-50A>G MANE Select	ENSP00000290866.4:n.1488-50A>G
ENST00000290866.9:c.1488-50A>G	ENSP00000290866.4:n.1488-50A>G
ENST00000428043.5:c.1488-50A>G	ENSP00000397593.2:n.1488-50A>G
ENST00000582678.5:c.*887-50A>G	ENSP00000462995.1:n.*887-50A>G
ENST00000584529.5:n.1377-50A>G
NM_000789.3:c.1488-50A>G	NP_000780.1:n.1488-50A>G
XM_005257110.1:c.939-50A>G	XP_005257167.1:n.939-50A>G
NM_000789.4:c.1488-50A>G MANE Select	NP_000780.1:n.1488-50A>G
NM_001382700.1:c.921-50A>G	NP_001369629.1:n.921-50A>G
NM_001382701.1:c.636-50A>G	NP_001369630.1:n.636-50A>G