Canonical Allele Identifier: CA501186741

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566028C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488667C>A , CM000679.2:g.63488667C>A	GRCh38
NC_000017.10:g.61566028C>A , CM000679.1:g.61566028C>A	GRCh37
NC_000017.9:g.58919760C>A	NCBI36
NG_011648.1:g.16595C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2325C>A MANE Select	ENSP00000290866.4:p.Ala775=
ENST00000290863.10:c.603C>A	ENSP00000290863.6:p.Ala201=
ENST00000290866.9:c.2325C>A	ENSP00000290866.4:p.Ala775=
ENST00000413513.7:c.603C>A	ENSP00000392247.3:p.Ala201=
ENST00000428043.5:c.2325C>A	ENSP00000397593.2:p.Ala775=
ENST00000577647.2:c.603C>A	ENSP00000464149.1:p.Ala201=
ENST00000578839.5:c.*395C>A	ENSP00000462110.2:n.*395C>A
ENST00000579204.1:c.584C>A	ENSP00000464629.1:n.584C>A
ENST00000579314.5:c.*54C>A	ENSP00000462599.1:n.*54C>A
ENST00000582005.5:c.*245C>A	ENSP00000462002.1:n.*245C>A
ENST00000582761.1:c.93C>A	ENSP00000462909.1:p.Ala31=
ENST00000584865.5:n.271C>A
NM_000789.3:c.2325C>A	NP_000780.1:p.Ala775=
NM_001178057.1:c.603C>A	NP_001171528.1:p.Ala201=
NM_152830.2:c.603C>A	NP_690043.1:p.Ala201=
XM_005257110.1:c.1776C>A	XP_005257167.1:p.Ala592=
XM_006721737.2:c.663C>A	XP_006721800.2:p.Ala221=
XM_006721737.3:c.663C>A	XP_006721800.2:p.Ala221=
NM_000789.4:c.2325C>A MANE Select	NP_000780.1:p.Ala775=
NM_001178057.2:c.603C>A	NP_001171528.1:p.Ala201=
NM_152830.3:c.603C>A	NP_690043.1:p.Ala201=
NM_001382700.1:c.1758C>A	NP_001369629.1:p.Ala586=
NM_001382701.1:c.1473C>A	NP_001369630.1:p.Ala491=
NM_001382702.1:c.255C>A	NP_001369631.1:p.Ala85=
NR_168483.1:n.703C>A