Canonical Allele Identifier: CA501341660

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61559887C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482526C>T , CM000679.2:g.63482526C>T	GRCh38
NC_000017.10:g.61559887C>T , CM000679.1:g.61559887C>T	GRCh37
NC_000017.9:g.58913619C>T	NCBI36
NG_011648.1:g.10454C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1179C>T MANE Select	ENSP00000290866.4:p.Gly393=
ENST00000290866.9:c.1179C>T	ENSP00000290866.4:p.Gly393=
ENST00000428043.5:c.1179C>T	ENSP00000397593.2:p.Gly393=
ENST00000582678.5:c.*578C>T	ENSP00000462995.1:n.*578C>T
ENST00000584529.5:n.1213C>T
NM_000789.3:c.1179C>T	NP_000780.1:p.Gly393=
XM_005257110.1:c.630C>T	XP_005257167.1:p.Gly210=
NM_000789.4:c.1179C>T MANE Select	NP_000780.1:p.Gly393=
NM_001382700.1:c.612C>T	NP_001369629.1:p.Gly204=
NM_001382701.1:c.327C>T	NP_001369630.1:p.Gly109=