Canonical Allele Identifier: CA400558162

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566322T>G (hg19) ; chr17:g.63488961T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488961T>G , CM000679.2:g.63488961T>G	GRCh38
NC_000017.10:g.61566322T>G , CM000679.1:g.61566322T>G	GRCh37
NC_000017.9:g.58920054T>G	NCBI36
NG_011648.1:g.16889T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2470T>G MANE Select	ENSP00000290866.4:p.Ser824Ala
ENST00000290863.10:c.748T>G	ENSP00000290863.6:p.Ser250Ala
ENST00000290866.9:c.2470T>G	ENSP00000290866.4:p.Ser824Ala
ENST00000413513.7:c.748T>G	ENSP00000392247.3:p.Ser250Ala
ENST00000428043.5:c.2470T>G	ENSP00000397593.2:p.Ser824Ala
ENST00000577647.2:c.748T>G	ENSP00000464149.1:p.Ser250Ala
ENST00000578839.5:c.*519+170T>G	ENSP00000462110.2:n.*519+170T>G
ENST00000579204.1:c.729T>G	ENSP00000464629.1:n.729T>G
ENST00000579314.5:c.*199T>G	ENSP00000462599.1:n.*199T>G
ENST00000582005.5:c.*390T>G	ENSP00000462002.1:n.*390T>G
ENST00000582761.1:c.238T>G	ENSP00000462909.1:p.Ser80Ala
ENST00000584865.5:n.416T>G
NM_000789.3:c.2470T>G	NP_000780.1:p.Ser824Ala
NM_001178057.1:c.748T>G	NP_001171528.1:p.Ser250Ala
NM_152830.2:c.748T>G	NP_690043.1:p.Ser250Ala
XM_005257110.1:c.1921T>G	XP_005257167.1:p.Ser641Ala
XM_006721737.2:c.808T>G	XP_006721800.2:p.Ser270Ala
XM_006721737.3:c.808T>G	XP_006721800.2:p.Ser270Ala
NM_000789.4:c.2470T>G MANE Select	NP_000780.1:p.Ser824Ala
NM_001178057.2:c.748T>G	NP_001171528.1:p.Ser250Ala
NM_152830.3:c.748T>G	NP_690043.1:p.Ser250Ala
NM_001382700.1:c.1903T>G	NP_001369629.1:p.Ser635Ala
NM_001382701.1:c.1618T>G	NP_001369630.1:p.Ser540Ala
NM_001382702.1:c.379+170T>G	NP_001369631.1:n.379+170T>G
NR_168483.1:n.848T>G