Canonical Allele Identifier: CA400568546

Gene: ACE

Linked Data

• gnomAD v4: 17-63497187-C-A
• MyVariant Identifiers: chr17:g.61574548C>A (hg19) ; chr17:g.63497187C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497187C>A , CM000679.2:g.63497187C>A	GRCh38
NC_000017.10:g.61574548C>A , CM000679.1:g.61574548C>A	GRCh37
NC_000017.9:g.58928280C>A	NCBI36
NG_011648.1:g.25115C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3742C>A MANE Select	ENSP00000290866.4:p.Leu1248Met
ENST00000290863.10:c.2020C>A	ENSP00000290863.6:p.Leu674Met
ENST00000290866.9:c.3742C>A	ENSP00000290866.4:p.Leu1248Met
ENST00000413513.7:c.1897C>A	ENSP00000392247.3:p.Leu633Met
ENST00000428043.5:c.*164C>A	ENSP00000397593.2:n.*164C>A
ENST00000577647.2:c.1969+202C>A	ENSP00000464149.1:n.1969+202C>A
ENST00000578839.5:c.*1497C>A	ENSP00000462110.2:n.*1497C>A
ENST00000579314.5:c.*1471C>A	ENSP00000462599.1:n.*1471C>A
NM_000789.3:c.3742C>A	NP_000780.1:p.Leu1248Met
NM_001178057.1:c.1897C>A	NP_001171528.1:p.Leu633Met
NM_152830.2:c.2020C>A	NP_690043.1:p.Leu674Met
XM_005257110.1:c.3193C>A	XP_005257167.1:p.Leu1065Met
XM_006721737.2:c.2080C>A	XP_006721800.2:p.Leu694Met
XM_006721737.3:c.2080C>A	XP_006721800.2:p.Leu694Met
NM_000789.4:c.3742C>A MANE Select	NP_000780.1:p.Leu1248Met
NM_001178057.2:c.1897C>A	NP_001171528.1:p.Leu633Met
NM_152830.3:c.2020C>A	NP_690043.1:p.Leu674Met
NM_001382700.1:c.3175C>A	NP_001369629.1:p.Leu1059Met
NM_001382701.1:c.2890C>A	NP_001369630.1:p.Leu964Met
NM_001382702.1:c.1357C>A	NP_001369631.1:p.Leu453Met
NR_168483.1:n.2120C>A