Canonical Allele Identifier: CA400557826

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566027C>G (hg19) ; chr17:g.63488666C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488666C>G , CM000679.2:g.63488666C>G	GRCh38
NC_000017.10:g.61566027C>G , CM000679.1:g.61566027C>G	GRCh37
NC_000017.9:g.58919759C>G	NCBI36
NG_011648.1:g.16594C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2324C>G MANE Select	ENSP00000290866.4:p.Ala775Gly
ENST00000290863.10:c.602C>G	ENSP00000290863.6:p.Ala201Gly
ENST00000290866.9:c.2324C>G	ENSP00000290866.4:p.Ala775Gly
ENST00000413513.7:c.602C>G	ENSP00000392247.3:p.Ala201Gly
ENST00000428043.5:c.2324C>G	ENSP00000397593.2:p.Ala775Gly
ENST00000577647.2:c.602C>G	ENSP00000464149.1:p.Ala201Gly
ENST00000578839.5:c.*394C>G	ENSP00000462110.2:n.*394C>G
ENST00000579204.1:c.583C>G	ENSP00000464629.1:n.583C>G
ENST00000579314.5:c.*53C>G	ENSP00000462599.1:n.*53C>G
ENST00000582005.5:c.*244C>G	ENSP00000462002.1:n.*244C>G
ENST00000582761.1:c.92C>G	ENSP00000462909.1:p.Ala31Gly
ENST00000584865.5:n.270C>G
NM_000789.3:c.2324C>G	NP_000780.1:p.Ala775Gly
NM_001178057.1:c.602C>G	NP_001171528.1:p.Ala201Gly
NM_152830.2:c.602C>G	NP_690043.1:p.Ala201Gly
XM_005257110.1:c.1775C>G	XP_005257167.1:p.Ala592Gly
XM_006721737.2:c.662C>G	XP_006721800.2:p.Ala221Gly
XM_006721737.3:c.662C>G	XP_006721800.2:p.Ala221Gly
NM_000789.4:c.2324C>G MANE Select	NP_000780.1:p.Ala775Gly
NM_001178057.2:c.602C>G	NP_001171528.1:p.Ala201Gly
NM_152830.3:c.602C>G	NP_690043.1:p.Ala201Gly
NM_001382700.1:c.1757C>G	NP_001369629.1:p.Ala586Gly
NM_001382701.1:c.1472C>G	NP_001369630.1:p.Ala491Gly
NM_001382702.1:c.254C>G	NP_001369631.1:p.Ala85Gly
NR_168483.1:n.702C>G