Canonical Allele Identifier: CA501341511

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61555411T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478050T>G , CM000679.2:g.63478050T>G	GRCh38
NC_000017.10:g.61555411T>G , CM000679.1:g.61555411T>G	GRCh37
NC_000017.9:g.58909143T>G	NCBI36
NG_011648.1:g.5978T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.369T>G MANE Select	ENSP00000290866.4:p.Ala123=
ENST00000290866.9:c.369T>G	ENSP00000290866.4:p.Ala123=
ENST00000428043.5:c.369T>G	ENSP00000397593.2:p.Ala123=
ENST00000579462.1:n.394T>G
ENST00000580318.1:n.558T>G
ENST00000582627.1:c.369T>G	ENSP00000462280.1:p.Ala123=
ENST00000582678.5:c.369T>G	ENSP00000462995.1:p.Ala123=
ENST00000583336.5:n.403T>G
ENST00000584529.5:n.403T>G
NM_000789.3:c.369T>G	NP_000780.1:p.Ala123=
XM_005257110.1:c.-87T>G	XP_005257167.1:n.-87T>G
NM_000789.4:c.369T>G MANE Select	NP_000780.1:p.Ala123=
NM_001382700.1:c.134T>G	NP_001369629.1:p.Leu45Arg
NM_001382701.1:c.-246T>G	NP_001369630.1:n.-246T>G