Canonical Allele Identifier: CA400567803

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574329A>G (hg19) ; chr17:g.63496968A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496968A>G , CM000679.2:g.63496968A>G	GRCh38
NC_000017.10:g.61574329A>G , CM000679.1:g.61574329A>G	GRCh37
NC_000017.9:g.58928061A>G	NCBI36
NG_011648.1:g.24896A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3674A>G MANE Select	ENSP00000290866.4:p.Asn1225Ser
ENST00000290863.10:c.1952A>G	ENSP00000290863.6:p.Asn651Ser
ENST00000290866.9:c.3674A>G	ENSP00000290866.4:p.Asn1225Ser
ENST00000413513.7:c.1829A>G	ENSP00000392247.3:p.Asn610Ser
ENST00000428043.5:c.3674A>G	ENSP00000397593.2:p.Asn1225Ser
ENST00000577418.5:n.684A>G
ENST00000577647.2:c.1952A>G	ENSP00000464149.1:p.Asn651Ser
ENST00000578839.5:c.*1429A>G	ENSP00000462110.2:n.*1429A>G
ENST00000579314.5:c.*1403A>G	ENSP00000462599.1:n.*1403A>G
ENST00000579409.1:c.361A>G
ENST00000582244.1:n.548A>G
NM_000789.3:c.3674A>G	NP_000780.1:p.Asn1225Ser
NM_001178057.1:c.1829A>G	NP_001171528.1:p.Asn610Ser
NM_152830.2:c.1952A>G	NP_690043.1:p.Asn651Ser
XM_005257110.1:c.3125A>G	XP_005257167.1:p.Asn1042Ser
XM_006721737.2:c.2012A>G	XP_006721800.2:p.Asn671Ser
XM_006721737.3:c.2012A>G	XP_006721800.2:p.Asn671Ser
NM_000789.4:c.3674A>G MANE Select	NP_000780.1:p.Asn1225Ser
NM_001178057.2:c.1829A>G	NP_001171528.1:p.Asn610Ser
NM_152830.3:c.1952A>G	NP_690043.1:p.Asn651Ser
NM_001382700.1:c.3107A>G	NP_001369629.1:p.Asn1036Ser
NM_001382701.1:c.2822A>G	NP_001369630.1:p.Asn941Ser
NM_001382702.1:c.1289A>G	NP_001369631.1:p.Asn430Ser
NR_168483.1:n.2052A>G