Canonical Allele Identifier: CA501187183

Gene: ACE

Linked Data

• dbSNP Id: rs2030161864
• MyVariant Identifiers: chr17:g.61566097C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488736C>T , CM000679.2:g.63488736C>T	GRCh38
NC_000017.10:g.61566097C>T , CM000679.1:g.61566097C>T	GRCh37
NC_000017.9:g.58919829C>T	NCBI36
NG_011648.1:g.16664C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2394C>T MANE Select	ENSP00000290866.4:p.Ile798=
ENST00000290863.10:c.672C>T	ENSP00000290863.6:p.Ile224=
ENST00000290866.9:c.2394C>T	ENSP00000290866.4:p.Ile798=
ENST00000413513.7:c.672C>T	ENSP00000392247.3:p.Ile224=
ENST00000428043.5:c.2394C>T	ENSP00000397593.2:p.Ile798=
ENST00000577647.2:c.672C>T	ENSP00000464149.1:p.Ile224=
ENST00000578839.5:c.*464C>T	ENSP00000462110.2:n.*464C>T
ENST00000579204.1:c.653C>T	ENSP00000464629.1:n.653C>T
ENST00000579314.5:c.*123C>T	ENSP00000462599.1:n.*123C>T
ENST00000582005.5:c.*314C>T	ENSP00000462002.1:n.*314C>T
ENST00000582761.1:c.162C>T	ENSP00000462909.1:p.Ile54=
ENST00000584865.5:n.340C>T
NM_000789.3:c.2394C>T	NP_000780.1:p.Ile798=
NM_001178057.1:c.672C>T	NP_001171528.1:p.Ile224=
NM_152830.2:c.672C>T	NP_690043.1:p.Ile224=
XM_005257110.1:c.1845C>T	XP_005257167.1:p.Ile615=
XM_006721737.2:c.732C>T	XP_006721800.2:p.Ile244=
XM_006721737.3:c.732C>T	XP_006721800.2:p.Ile244=
NM_000789.4:c.2394C>T MANE Select	NP_000780.1:p.Ile798=
NM_001178057.2:c.672C>T	NP_001171528.1:p.Ile224=
NM_152830.3:c.672C>T	NP_690043.1:p.Ile224=
NM_001382700.1:c.1827C>T	NP_001369629.1:p.Ile609=
NM_001382701.1:c.1542C>T	NP_001369630.1:p.Ile514=
NM_001382702.1:c.324C>T	NP_001369631.1:p.Ile108=
NR_168483.1:n.772C>T