Canonical Allele Identifier: CA501342393

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574626C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497265C>T , CM000679.2:g.63497265C>T	GRCh38
NC_000017.10:g.61574626C>T , CM000679.1:g.61574626C>T	GRCh37
NC_000017.9:g.58928358C>T	NCBI36
NG_011648.1:g.25193C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3820C>T MANE Select	ENSP00000290866.4:p.Leu1274=
ENST00000290863.10:c.2098C>T	ENSP00000290863.6:p.Leu700=
ENST00000290866.9:c.3820C>T	ENSP00000290866.4:p.Leu1274=
ENST00000413513.7:c.1975C>T	ENSP00000392247.3:p.Leu659=
ENST00000428043.5:c.*242C>T	ENSP00000397593.2:n.*242C>T
ENST00000577647.2:c.1969+280C>T	ENSP00000464149.1:n.1969+280C>T
ENST00000578839.5:c.*1575C>T	ENSP00000462110.2:n.*1575C>T
ENST00000579314.5:c.*1549C>T	ENSP00000462599.1:n.*1549C>T
NM_000789.3:c.3820C>T	NP_000780.1:p.Leu1274=
NM_001178057.1:c.1975C>T	NP_001171528.1:p.Leu659=
NM_152830.2:c.2098C>T	NP_690043.1:p.Leu700=
XM_005257110.1:c.3271C>T	XP_005257167.1:p.Leu1091=
XM_006721737.2:c.2158C>T	XP_006721800.2:p.Leu720=
XM_006721737.3:c.2158C>T	XP_006721800.2:p.Leu720=
NM_000789.4:c.3820C>T MANE Select	NP_000780.1:p.Leu1274=
NM_001178057.2:c.1975C>T	NP_001171528.1:p.Leu659=
NM_152830.3:c.2098C>T	NP_690043.1:p.Leu700=
NM_001382700.1:c.3253C>T	NP_001369629.1:p.Leu1085=
NM_001382701.1:c.2968C>T	NP_001369630.1:p.Leu990=
NM_001382702.1:c.1435C>T	NP_001369631.1:p.Leu479=
NR_168483.1:n.2198C>T