Canonical Allele Identifier: CA501341443

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61555300A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477939A>G , CM000679.2:g.63477939A>G	GRCh38
NC_000017.10:g.61555300A>G , CM000679.1:g.61555300A>G	GRCh37
NC_000017.9:g.58909032A>G	NCBI36
NG_011648.1:g.5867A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.258A>G MANE Select	ENSP00000290866.4:p.Ala86=
ENST00000290866.9:c.258A>G	ENSP00000290866.4:p.Ala86=
ENST00000428043.5:c.258A>G	ENSP00000397593.2:p.Ala86=
ENST00000579462.1:n.283A>G
ENST00000580318.1:n.447A>G
ENST00000582627.1:c.258A>G	ENSP00000462280.1:p.Ala86=
ENST00000582678.5:c.258A>G	ENSP00000462995.1:p.Ala86=
ENST00000583336.5:n.292A>G
ENST00000584529.5:n.292A>G
NM_000789.3:c.258A>G	NP_000780.1:p.Ala86=
XM_005257110.1:c.-198A>G	XP_005257167.1:n.-198A>G
NM_000789.4:c.258A>G MANE Select	NP_000780.1:p.Ala86=
NM_001382700.1:c.23A>G	NP_001369629.1:p.Gln8Arg
NM_001382701.1:c.-357A>G	NP_001369630.1:n.-357A>G