Canonical Allele Identifier: CA400567580

Gene: ACE

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3643C>A MANE Select	ENSP00000290866.4:p.His1215Asn
ENST00000290863.10:c.1921C>A	ENSP00000290863.6:p.His641Asn
ENST00000290866.9:c.3643C>A	ENSP00000290866.4:p.His1215Asn
ENST00000413513.7:c.1798C>A	ENSP00000392247.3:p.His600Asn
ENST00000428043.5:c.3643C>A	ENSP00000397593.2:p.His1215Asn
ENST00000577418.5:n.653C>A
ENST00000577647.2:c.1921C>A	ENSP00000464149.1:p.His641Asn
ENST00000578839.5:c.*1398C>A	ENSP00000462110.2:n.*1398C>A
ENST00000579314.5:c.*1372C>A	ENSP00000462599.1:n.*1372C>A
ENST00000579409.1:c.330C>A
ENST00000582244.1:n.517C>A
NM_000789.3:c.3643C>A	NP_000780.1:p.His1215Asn
NM_001178057.1:c.1798C>A	NP_001171528.1:p.His600Asn
NM_152830.2:c.1921C>A	NP_690043.1:p.His641Asn
XM_005257110.1:c.3094C>A	XP_005257167.1:p.His1032Asn
XM_006721737.2:c.1981C>A	XP_006721800.2:p.His661Asn
XM_006721737.3:c.1981C>A	XP_006721800.2:p.His661Asn
NM_000789.4:c.3643C>A MANE Select	NP_000780.1:p.His1215Asn
NM_001178057.2:c.1798C>A	NP_001171528.1:p.His600Asn
NM_152830.3:c.1921C>A	NP_690043.1:p.His641Asn
NM_001382700.1:c.3076C>A	NP_001369629.1:p.His1026Asn
NM_001382701.1:c.2791C>A	NP_001369630.1:p.His931Asn
NM_001382702.1:c.1258C>A	NP_001369631.1:p.His420Asn
NR_168483.1:n.2021C>A