Canonical Allele Identifier: CA400558220

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566350C>A (hg19) ; chr17:g.63488989C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488989C>A , CM000679.2:g.63488989C>A	GRCh38
NC_000017.10:g.61566350C>A , CM000679.1:g.61566350C>A	GRCh37
NC_000017.9:g.58920082C>A	NCBI36
NG_011648.1:g.16917C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2498C>A MANE Select	ENSP00000290866.4:p.Ser833Tyr
ENST00000290863.10:c.776C>A	ENSP00000290863.6:p.Ser259Tyr
ENST00000290866.9:c.2498C>A	ENSP00000290866.4:p.Ser833Tyr
ENST00000413513.7:c.776C>A	ENSP00000392247.3:p.Ser259Tyr
ENST00000428043.5:c.2498C>A	ENSP00000397593.2:p.Ser833Tyr
ENST00000577647.2:c.776C>A	ENSP00000464149.1:p.Ser259Tyr
ENST00000578839.5:c.*519+198C>A	ENSP00000462110.2:n.*519+198C>A
ENST00000579204.1:c.757C>A	ENSP00000464629.1:n.757C>A
ENST00000579314.5:c.*227C>A	ENSP00000462599.1:n.*227C>A
ENST00000582005.5:c.*418C>A	ENSP00000462002.1:n.*418C>A
ENST00000582761.1:c.266C>A	ENSP00000462909.1:p.Ser89Tyr
ENST00000584865.5:n.444C>A
NM_000789.3:c.2498C>A	NP_000780.1:p.Ser833Tyr
NM_001178057.1:c.776C>A	NP_001171528.1:p.Ser259Tyr
NM_152830.2:c.776C>A	NP_690043.1:p.Ser259Tyr
XM_005257110.1:c.1949C>A	XP_005257167.1:p.Ser650Tyr
XM_006721737.2:c.836C>A	XP_006721800.2:p.Ser279Tyr
XM_006721737.3:c.836C>A	XP_006721800.2:p.Ser279Tyr
NM_000789.4:c.2498C>A MANE Select	NP_000780.1:p.Ser833Tyr
NM_001178057.2:c.776C>A	NP_001171528.1:p.Ser259Tyr
NM_152830.3:c.776C>A	NP_690043.1:p.Ser259Tyr
NM_001382700.1:c.1931C>A	NP_001369629.1:p.Ser644Tyr
NM_001382701.1:c.1646C>A	NP_001369630.1:p.Ser549Tyr
NM_001382702.1:c.379+198C>A	NP_001369631.1:n.379+198C>A
NR_168483.1:n.876C>A