Canonical Allele Identifier: CA8700134

Gene: ACE

Linked Data

• ClinVar Variation Id: 324397
• ClinVar RCV Id: RCV000349387
• dbSNP Id: rs35580653
• ExAC: 17:61566339 C / T
• gnomAD v2: 17-61566339-C-T
• gnomAD v3: 17-63488978-C-T
• gnomAD v4: 17-63488978-C-T
• MyVariant Identifiers: chr17:g.61566339C>T (hg19) ; chr17:g.63488978C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488978C>T , CM000679.2:g.63488978C>T	GRCh38
NC_000017.10:g.61566339C>T , CM000679.1:g.61566339C>T	GRCh37
NC_000017.9:g.58920071C>T	NCBI36
NG_011648.1:g.16906C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2487C>T MANE Select	ENSP00000290866.4:p.Tyr829=
ENST00000290863.10:c.765C>T	ENSP00000290863.6:p.Tyr255=
ENST00000290866.9:c.2487C>T	ENSP00000290866.4:p.Tyr829=
ENST00000413513.7:c.765C>T	ENSP00000392247.3:p.Tyr255=
ENST00000428043.5:c.2487C>T	ENSP00000397593.2:p.Tyr829=
ENST00000577647.2:c.765C>T	ENSP00000464149.1:p.Tyr255=
ENST00000578839.5:c.*519+187C>T	ENSP00000462110.2:n.*519+187C>T
ENST00000579204.1:c.746C>T	ENSP00000464629.1:n.746C>T
ENST00000579314.5:c.*216C>T	ENSP00000462599.1:n.*216C>T
ENST00000582005.5:c.*407C>T	ENSP00000462002.1:n.*407C>T
ENST00000582761.1:c.255C>T	ENSP00000462909.1:p.Tyr85=
ENST00000584865.5:n.433C>T
NM_000789.3:c.2487C>T	NP_000780.1:p.Tyr829=
NM_001178057.1:c.765C>T	NP_001171528.1:p.Tyr255=
NM_152830.2:c.765C>T	NP_690043.1:p.Tyr255=
XM_005257110.1:c.1938C>T	XP_005257167.1:p.Tyr646=
XM_006721737.2:c.825C>T	XP_006721800.2:p.Tyr275=
XM_006721737.3:c.825C>T	XP_006721800.2:p.Tyr275=
NM_000789.4:c.2487C>T MANE Select	NP_000780.1:p.Tyr829=
NM_001178057.2:c.765C>T	NP_001171528.1:p.Tyr255=
NM_152830.3:c.765C>T	NP_690043.1:p.Tyr255=
NM_001382700.1:c.1920C>T	NP_001369629.1:p.Tyr640=
NM_001382701.1:c.1635C>T	NP_001369630.1:p.Tyr545=
NM_001382702.1:c.379+187C>T	NP_001369631.1:n.379+187C>T
NR_168483.1:n.865C>T