Canonical Allele Identifier: CA400558496

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566399C>G (hg19) ; chr17:g.63489038C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63489038C>G , CM000679.2:g.63489038C>G	GRCh38
NC_000017.10:g.61566399C>G , CM000679.1:g.61566399C>G	GRCh37
NC_000017.9:g.58920131C>G	NCBI36
NG_011648.1:g.16966C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2547C>G MANE Select	ENSP00000290866.4:p.Tyr849Ter
ENST00000290863.10:c.825C>G	ENSP00000290863.6:p.Tyr275Ter
ENST00000290866.9:c.2547C>G	ENSP00000290866.4:p.Tyr849Ter
ENST00000413513.7:c.825C>G	ENSP00000392247.3:p.Tyr275Ter
ENST00000428043.5:c.2547C>G	ENSP00000397593.2:p.Tyr849Ter
ENST00000577647.2:c.825C>G	ENSP00000464149.1:p.Tyr275Ter
ENST00000578839.5:c.*519+247C>G	ENSP00000462110.2:n.*519+247C>G
ENST00000579204.1:c.806C>G	ENSP00000464629.1:n.806C>G
ENST00000579314.5:c.*276C>G	ENSP00000462599.1:n.*276C>G
ENST00000582005.5:c.*467C>G	ENSP00000462002.1:n.*467C>G
ENST00000582761.1:c.315C>G	ENSP00000462909.1:p.Tyr105Ter
ENST00000584865.5:n.493C>G
NM_000789.3:c.2547C>G	NP_000780.1:p.Tyr849Ter
NM_001178057.1:c.825C>G	NP_001171528.1:p.Tyr275Ter
NM_152830.2:c.825C>G	NP_690043.1:p.Tyr275Ter
XM_005257110.1:c.1998C>G	XP_005257167.1:p.Tyr666Ter
XM_006721737.2:c.885C>G	XP_006721800.2:p.Tyr295Ter
XM_006721737.3:c.885C>G	XP_006721800.2:p.Tyr295Ter
NM_000789.4:c.2547C>G MANE Select	NP_000780.1:p.Tyr849Ter
NM_001178057.2:c.825C>G	NP_001171528.1:p.Tyr275Ter
NM_152830.3:c.825C>G	NP_690043.1:p.Tyr275Ter
NM_001382700.1:c.1980C>G	NP_001369629.1:p.Tyr660Ter
NM_001382701.1:c.1695C>G	NP_001369630.1:p.Tyr565Ter
NM_001382702.1:c.379+247C>G	NP_001369631.1:n.379+247C>G
NR_168483.1:n.925C>G