Canonical Allele Identifier: CA400567583

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574298C>G (hg19) ; chr17:g.63496937C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496937C>G , CM000679.2:g.63496937C>G	GRCh38
NC_000017.10:g.61574298C>G , CM000679.1:g.61574298C>G	GRCh37
NC_000017.9:g.58928030C>G	NCBI36
NG_011648.1:g.24865C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3643C>G MANE Select	ENSP00000290866.4:p.His1215Asp
ENST00000290863.10:c.1921C>G	ENSP00000290863.6:p.His641Asp
ENST00000290866.9:c.3643C>G	ENSP00000290866.4:p.His1215Asp
ENST00000413513.7:c.1798C>G	ENSP00000392247.3:p.His600Asp
ENST00000428043.5:c.3643C>G	ENSP00000397593.2:p.His1215Asp
ENST00000577418.5:n.653C>G
ENST00000577647.2:c.1921C>G	ENSP00000464149.1:p.His641Asp
ENST00000578839.5:c.*1398C>G	ENSP00000462110.2:n.*1398C>G
ENST00000579314.5:c.*1372C>G	ENSP00000462599.1:n.*1372C>G
ENST00000579409.1:c.330C>G
ENST00000582244.1:n.517C>G
NM_000789.3:c.3643C>G	NP_000780.1:p.His1215Asp
NM_001178057.1:c.1798C>G	NP_001171528.1:p.His600Asp
NM_152830.2:c.1921C>G	NP_690043.1:p.His641Asp
XM_005257110.1:c.3094C>G	XP_005257167.1:p.His1032Asp
XM_006721737.2:c.1981C>G	XP_006721800.2:p.His661Asp
XM_006721737.3:c.1981C>G	XP_006721800.2:p.His661Asp
NM_000789.4:c.3643C>G MANE Select	NP_000780.1:p.His1215Asp
NM_001178057.2:c.1798C>G	NP_001171528.1:p.His600Asp
NM_152830.3:c.1921C>G	NP_690043.1:p.His641Asp
NM_001382700.1:c.3076C>G	NP_001369629.1:p.His1026Asp
NM_001382701.1:c.2791C>G	NP_001369630.1:p.His931Asp
NM_001382702.1:c.1258C>G	NP_001369631.1:p.His420Asp
NR_168483.1:n.2021C>G