Canonical Allele Identifier: CA501186905

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566061A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488700A>G , CM000679.2:g.63488700A>G	GRCh38
NC_000017.10:g.61566061A>G , CM000679.1:g.61566061A>G	GRCh37
NC_000017.9:g.58919793A>G	NCBI36
NG_011648.1:g.16628A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2358A>G MANE Select	ENSP00000290866.4:p.Ala786=
ENST00000290863.10:c.636A>G	ENSP00000290863.6:p.Ala212=
ENST00000290866.9:c.2358A>G	ENSP00000290866.4:p.Ala786=
ENST00000413513.7:c.636A>G	ENSP00000392247.3:p.Ala212=
ENST00000428043.5:c.2358A>G	ENSP00000397593.2:p.Ala786=
ENST00000577647.2:c.636A>G	ENSP00000464149.1:p.Ala212=
ENST00000578839.5:c.*428A>G	ENSP00000462110.2:n.*428A>G
ENST00000579204.1:c.617A>G	ENSP00000464629.1:n.617A>G
ENST00000579314.5:c.*87A>G	ENSP00000462599.1:n.*87A>G
ENST00000582005.5:c.*278A>G	ENSP00000462002.1:n.*278A>G
ENST00000582761.1:c.126A>G	ENSP00000462909.1:p.Ala42=
ENST00000584865.5:n.304A>G
NM_000789.3:c.2358A>G	NP_000780.1:p.Ala786=
NM_001178057.1:c.636A>G	NP_001171528.1:p.Ala212=
NM_152830.2:c.636A>G	NP_690043.1:p.Ala212=
XM_005257110.1:c.1809A>G	XP_005257167.1:p.Ala603=
XM_006721737.2:c.696A>G	XP_006721800.2:p.Ala232=
XM_006721737.3:c.696A>G	XP_006721800.2:p.Ala232=
NM_000789.4:c.2358A>G MANE Select	NP_000780.1:p.Ala786=
NM_001178057.2:c.636A>G	NP_001171528.1:p.Ala212=
NM_152830.3:c.636A>G	NP_690043.1:p.Ala212=
NM_001382700.1:c.1791A>G	NP_001369629.1:p.Ala597=
NM_001382701.1:c.1506A>G	NP_001369630.1:p.Ala502=
NM_001382702.1:c.288A>G	NP_001369631.1:p.Ala96=
NR_168483.1:n.736A>G