Canonical Allele Identifier: CA501342279

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574177C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496816C>A , CM000679.2:g.63496816C>A	GRCh38
NC_000017.10:g.61574177C>A , CM000679.1:g.61574177C>A	GRCh37
NC_000017.9:g.58927909C>A	NCBI36
NG_011648.1:g.24744C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3522C>A MANE Select	ENSP00000290866.4:p.Gly1174=
ENST00000290863.10:c.1800C>A	ENSP00000290863.6:p.Gly600=
ENST00000290866.9:c.3522C>A	ENSP00000290866.4:p.Gly1174=
ENST00000413513.7:c.1677C>A	ENSP00000392247.3:p.Gly559=
ENST00000428043.5:c.3522C>A	ENSP00000397593.2:p.Gly1174=
ENST00000577418.5:n.532C>A
ENST00000577647.2:c.1800C>A	ENSP00000464149.1:p.Gly600=
ENST00000578839.5:c.*1277C>A	ENSP00000462110.2:n.*1277C>A
ENST00000579314.5:c.*1251C>A	ENSP00000462599.1:n.*1251C>A
ENST00000579409.1:c.209C>A
ENST00000582244.1:n.396C>A
NM_000789.3:c.3522C>A	NP_000780.1:p.Gly1174=
NM_001178057.1:c.1677C>A	NP_001171528.1:p.Gly559=
NM_152830.2:c.1800C>A	NP_690043.1:p.Gly600=
XM_005257110.1:c.2973C>A	XP_005257167.1:p.Gly991=
XM_006721737.2:c.1860C>A	XP_006721800.2:p.Gly620=
XM_006721737.3:c.1860C>A	XP_006721800.2:p.Gly620=
NM_000789.4:c.3522C>A MANE Select	NP_000780.1:p.Gly1174=
NM_001178057.2:c.1677C>A	NP_001171528.1:p.Gly559=
NM_152830.3:c.1800C>A	NP_690043.1:p.Gly600=
NM_001382700.1:c.2955C>A	NP_001369629.1:p.Gly985=
NM_001382701.1:c.2670C>A	NP_001369630.1:p.Gly890=
NM_001382702.1:c.1137C>A	NP_001369631.1:p.Gly379=
NR_168483.1:n.1900C>A