Canonical Allele Identifier: CA501187151

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566094C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488733C>T , CM000679.2:g.63488733C>T	GRCh38
NC_000017.10:g.61566094C>T , CM000679.1:g.61566094C>T	GRCh37
NC_000017.9:g.58919826C>T	NCBI36
NG_011648.1:g.16661C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2391C>T MANE Select	ENSP00000290866.4:p.Ala797=
ENST00000290863.10:c.669C>T	ENSP00000290863.6:p.Ala223=
ENST00000290866.9:c.2391C>T	ENSP00000290866.4:p.Ala797=
ENST00000413513.7:c.669C>T	ENSP00000392247.3:p.Ala223=
ENST00000428043.5:c.2391C>T	ENSP00000397593.2:p.Ala797=
ENST00000577647.2:c.669C>T	ENSP00000464149.1:p.Ala223=
ENST00000578839.5:c.*461C>T	ENSP00000462110.2:n.*461C>T
ENST00000579204.1:c.650C>T	ENSP00000464629.1:n.650C>T
ENST00000579314.5:c.*120C>T	ENSP00000462599.1:n.*120C>T
ENST00000582005.5:c.*311C>T	ENSP00000462002.1:n.*311C>T
ENST00000582761.1:c.159C>T	ENSP00000462909.1:p.Ala53=
ENST00000584865.5:n.337C>T
NM_000789.3:c.2391C>T	NP_000780.1:p.Ala797=
NM_001178057.1:c.669C>T	NP_001171528.1:p.Ala223=
NM_152830.2:c.669C>T	NP_690043.1:p.Ala223=
XM_005257110.1:c.1842C>T	XP_005257167.1:p.Ala614=
XM_006721737.2:c.729C>T	XP_006721800.2:p.Ala243=
XM_006721737.3:c.729C>T	XP_006721800.2:p.Ala243=
NM_000789.4:c.2391C>T MANE Select	NP_000780.1:p.Ala797=
NM_001178057.2:c.669C>T	NP_001171528.1:p.Ala223=
NM_152830.3:c.669C>T	NP_690043.1:p.Ala223=
NM_001382700.1:c.1824C>T	NP_001369629.1:p.Ala608=
NM_001382701.1:c.1539C>T	NP_001369630.1:p.Ala513=
NM_001382702.1:c.321C>T	NP_001369631.1:p.Ala107=
NR_168483.1:n.769C>T