Canonical Allele Identifier: CA400568350

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574513C>G (hg19) ; chr17:g.63497152C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497152C>G , CM000679.2:g.63497152C>G	GRCh38
NC_000017.10:g.61574513C>G , CM000679.1:g.61574513C>G	GRCh37
NC_000017.9:g.58928245C>G	NCBI36
NG_011648.1:g.25080C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3707C>G MANE Select	ENSP00000290866.4:p.Pro1236Arg
ENST00000290863.10:c.1985C>G	ENSP00000290863.6:p.Pro662Arg
ENST00000290866.9:c.3707C>G	ENSP00000290866.4:p.Pro1236Arg
ENST00000413513.7:c.1862C>G	ENSP00000392247.3:p.Pro621Arg
ENST00000428043.5:c.*129C>G	ENSP00000397593.2:n.*129C>G
ENST00000577418.5:n.717C>G
ENST00000577647.2:c.1969+167C>G	ENSP00000464149.1:n.1969+167C>G
ENST00000578839.5:c.*1462C>G	ENSP00000462110.2:n.*1462C>G
ENST00000579314.5:c.*1436C>G	ENSP00000462599.1:n.*1436C>G
ENST00000579409.1:c.545C>G
NM_000789.3:c.3707C>G	NP_000780.1:p.Pro1236Arg
NM_001178057.1:c.1862C>G	NP_001171528.1:p.Pro621Arg
NM_152830.2:c.1985C>G	NP_690043.1:p.Pro662Arg
XM_005257110.1:c.3158C>G	XP_005257167.1:p.Pro1053Arg
XM_006721737.2:c.2045C>G	XP_006721800.2:p.Pro682Arg
XM_006721737.3:c.2045C>G	XP_006721800.2:p.Pro682Arg
NM_000789.4:c.3707C>G MANE Select	NP_000780.1:p.Pro1236Arg
NM_001178057.2:c.1862C>G	NP_001171528.1:p.Pro621Arg
NM_152830.3:c.1985C>G	NP_690043.1:p.Pro662Arg
NM_001382700.1:c.3140C>G	NP_001369629.1:p.Pro1047Arg
NM_001382701.1:c.2855C>G	NP_001369630.1:p.Pro952Arg
NM_001382702.1:c.1322C>G	NP_001369631.1:p.Pro441Arg
NR_168483.1:n.2085C>G