Canonical Allele Identifier: CA400556602

Gene: ACE

Linked Data

• dbSNP Id: rs1401450584
• gnomAD v2: 17-61564358-C-G
• gnomAD v4: 17-63486997-C-G
• MyVariant Identifiers: chr17:g.61564358C>G (hg19) ; chr17:g.63486997C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486997C>G , CM000679.2:g.63486997C>G	GRCh38
NC_000017.10:g.61564358C>G , CM000679.1:g.61564358C>G	GRCh37
NC_000017.9:g.58918090C>G	NCBI36
NG_011648.1:g.14925C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2229C>G MANE Select	ENSP00000290866.4:p.Ile743Met
ENST00000290863.10:c.507C>G	ENSP00000290863.6:p.Ile169Met
ENST00000290866.9:c.2229C>G	ENSP00000290866.4:p.Ile743Met
ENST00000413513.7:c.507C>G	ENSP00000392247.3:p.Ile169Met
ENST00000428043.5:c.2229C>G	ENSP00000397593.2:p.Ile743Met
ENST00000577647.2:c.507C>G	ENSP00000464149.1:p.Ile169Met
ENST00000578839.5:c.*299C>G	ENSP00000462110.2:n.*299C>G
ENST00000579204.1:c.410C>G	ENSP00000464629.1:n.410C>G
ENST00000579314.5:c.507C>G	ENSP00000462599.1:p.Ile169Met
ENST00000579726.5:c.791C>G
ENST00000582005.5:c.*149C>G	ENSP00000462002.1:n.*149C>G
ENST00000584865.5:n.175C>G
NM_000789.3:c.2229C>G	NP_000780.1:p.Ile743Met
NM_001178057.1:c.507C>G	NP_001171528.1:p.Ile169Met
NM_152830.2:c.507C>G	NP_690043.1:p.Ile169Met
XM_005257110.1:c.1680C>G	XP_005257167.1:p.Ile560Met
XM_006721737.2:c.567C>G	XP_006721800.2:p.Ile189Met
XM_006721737.3:c.567C>G	XP_006721800.2:p.Ile189Met
NM_000789.4:c.2229C>G MANE Select	NP_000780.1:p.Ile743Met
NM_001178057.2:c.507C>G	NP_001171528.1:p.Ile169Met
NM_152830.3:c.507C>G	NP_690043.1:p.Ile169Met
NM_001382700.1:c.1662C>G	NP_001369629.1:p.Ile554Met
NM_001382701.1:c.1377C>G	NP_001369630.1:p.Ile459Met
NM_001382702.1:c.159C>G	NP_001369631.1:p.Ile53Met
NR_168483.1:n.529C>G