Canonical Allele Identifier: CA400568971

Gene: ACE

Linked Data

• gnomAD v4: 17-63497253-C-A
• MyVariant Identifiers: chr17:g.61574614C>A (hg19) ; chr17:g.63497253C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497253C>A , CM000679.2:g.63497253C>A	GRCh38
NC_000017.10:g.61574614C>A , CM000679.1:g.61574614C>A	GRCh37
NC_000017.9:g.58928346C>A	NCBI36
NG_011648.1:g.25181C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3808C>A MANE Select	ENSP00000290866.4:p.Leu1270Met
ENST00000290863.10:c.2086C>A	ENSP00000290863.6:p.Leu696Met
ENST00000290866.9:c.3808C>A	ENSP00000290866.4:p.Leu1270Met
ENST00000413513.7:c.1963C>A	ENSP00000392247.3:p.Leu655Met
ENST00000428043.5:c.*230C>A	ENSP00000397593.2:n.*230C>A
ENST00000577647.2:c.1969+268C>A	ENSP00000464149.1:n.1969+268C>A
ENST00000578839.5:c.*1563C>A	ENSP00000462110.2:n.*1563C>A
ENST00000579314.5:c.*1537C>A	ENSP00000462599.1:n.*1537C>A
NM_000789.3:c.3808C>A	NP_000780.1:p.Leu1270Met
NM_001178057.1:c.1963C>A	NP_001171528.1:p.Leu655Met
NM_152830.2:c.2086C>A	NP_690043.1:p.Leu696Met
XM_005257110.1:c.3259C>A	XP_005257167.1:p.Leu1087Met
XM_006721737.2:c.2146C>A	XP_006721800.2:p.Leu716Met
XM_006721737.3:c.2146C>A	XP_006721800.2:p.Leu716Met
NM_000789.4:c.3808C>A MANE Select	NP_000780.1:p.Leu1270Met
NM_001178057.2:c.1963C>A	NP_001171528.1:p.Leu655Met
NM_152830.3:c.2086C>A	NP_690043.1:p.Leu696Met
NM_001382700.1:c.3241C>A	NP_001369629.1:p.Leu1081Met
NM_001382701.1:c.2956C>A	NP_001369630.1:p.Leu986Met
NM_001382702.1:c.1423C>A	NP_001369631.1:p.Leu475Met
NR_168483.1:n.2186C>A