Canonical Allele Identifier: CA400567370

Gene: ACE

Linked Data

• gnomAD v4: 17-63496902-C-G
• MyVariant Identifiers: chr17:g.61574263C>G (hg19) ; chr17:g.63496902C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496902C>G , CM000679.2:g.63496902C>G	GRCh38
NC_000017.10:g.61574263C>G , CM000679.1:g.61574263C>G	GRCh37
NC_000017.9:g.58927995C>G	NCBI36
NG_011648.1:g.24830C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3608C>G MANE Select	ENSP00000290866.4:p.Pro1203Arg
ENST00000290863.10:c.1886C>G	ENSP00000290863.6:p.Pro629Arg
ENST00000290866.9:c.3608C>G	ENSP00000290866.4:p.Pro1203Arg
ENST00000413513.7:c.1763C>G	ENSP00000392247.3:p.Pro588Arg
ENST00000428043.5:c.3608C>G	ENSP00000397593.2:p.Pro1203Arg
ENST00000577418.5:n.618C>G
ENST00000577647.2:c.1886C>G	ENSP00000464149.1:p.Pro629Arg
ENST00000578839.5:c.*1363C>G	ENSP00000462110.2:n.*1363C>G
ENST00000579314.5:c.*1337C>G	ENSP00000462599.1:n.*1337C>G
ENST00000579409.1:c.295C>G
ENST00000582244.1:n.482C>G
NM_000789.3:c.3608C>G	NP_000780.1:p.Pro1203Arg
NM_001178057.1:c.1763C>G	NP_001171528.1:p.Pro588Arg
NM_152830.2:c.1886C>G	NP_690043.1:p.Pro629Arg
XM_005257110.1:c.3059C>G	XP_005257167.1:p.Pro1020Arg
XM_006721737.2:c.1946C>G	XP_006721800.2:p.Pro649Arg
XM_006721737.3:c.1946C>G	XP_006721800.2:p.Pro649Arg
NM_000789.4:c.3608C>G MANE Select	NP_000780.1:p.Pro1203Arg
NM_001178057.2:c.1763C>G	NP_001171528.1:p.Pro588Arg
NM_152830.3:c.1886C>G	NP_690043.1:p.Pro629Arg
NM_001382700.1:c.3041C>G	NP_001369629.1:p.Pro1014Arg
NM_001382701.1:c.2756C>G	NP_001369630.1:p.Pro919Arg
NM_001382702.1:c.1223C>G	NP_001369631.1:p.Pro408Arg
NR_168483.1:n.1986C>G