Canonical Allele Identifier: CA400556134

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564017A>G (hg19) ; chr17:g.63486656A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486656A>G , CM000679.2:g.63486656A>G	GRCh38
NC_000017.10:g.61564017A>G , CM000679.1:g.61564017A>G	GRCh37
NC_000017.9:g.58917749A>G	NCBI36
NG_011648.1:g.14584A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2158A>G MANE Select	ENSP00000290866.4:p.Ile720Val
ENST00000290863.10:c.436A>G	ENSP00000290863.6:p.Ile146Val
ENST00000290866.9:c.2158A>G	ENSP00000290866.4:p.Ile720Val
ENST00000413513.7:c.436A>G	ENSP00000392247.3:p.Ile146Val
ENST00000428043.5:c.2158A>G	ENSP00000397593.2:p.Ile720Val
ENST00000577647.2:c.436A>G	ENSP00000464149.1:p.Ile146Val
ENST00000578839.5:c.*228A>G	ENSP00000462110.2:n.*228A>G
ENST00000579204.1:c.339A>G	ENSP00000464629.1:n.339A>G
ENST00000579314.5:c.436A>G	ENSP00000462599.1:p.Ile146Val
ENST00000579726.5:c.720A>G
ENST00000582005.5:c.*78A>G	ENSP00000462002.1:n.*78A>G
NM_000789.3:c.2158A>G	NP_000780.1:p.Ile720Val
NM_001178057.1:c.436A>G	NP_001171528.1:p.Ile146Val
NM_152830.2:c.436A>G	NP_690043.1:p.Ile146Val
XM_005257110.1:c.1609A>G	XP_005257167.1:p.Ile537Val
XM_006721737.2:c.496A>G	XP_006721800.2:p.Ile166Val
XM_006721737.3:c.496A>G	XP_006721800.2:p.Ile166Val
NM_000789.4:c.2158A>G MANE Select	NP_000780.1:p.Ile720Val
NM_001178057.2:c.436A>G	NP_001171528.1:p.Ile146Val
NM_152830.3:c.436A>G	NP_690043.1:p.Ile146Val
NM_001382700.1:c.1591A>G	NP_001369629.1:p.Ile531Val
NM_001382701.1:c.1306A>G	NP_001369630.1:p.Ile436Val
NM_001382702.1:c.88A>G	NP_001369631.1:p.Ile30Val
NR_168483.1:n.458A>G