Canonical Allele Identifier: CA400568460

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574534T>A (hg19) ; chr17:g.63497173T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497173T>A , CM000679.2:g.63497173T>A	GRCh38
NC_000017.10:g.61574534T>A , CM000679.1:g.61574534T>A	GRCh37
NC_000017.9:g.58928266T>A	NCBI36
NG_011648.1:g.25101T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3728T>A MANE Select	ENSP00000290866.4:p.Val1243Asp
ENST00000290863.10:c.2006T>A	ENSP00000290863.6:p.Val669Asp
ENST00000290866.9:c.3728T>A	ENSP00000290866.4:p.Val1243Asp
ENST00000413513.7:c.1883T>A	ENSP00000392247.3:p.Val628Asp
ENST00000428043.5:c.*150T>A	ENSP00000397593.2:n.*150T>A
ENST00000577647.2:c.1969+188T>A	ENSP00000464149.1:n.1969+188T>A
ENST00000578839.5:c.*1483T>A	ENSP00000462110.2:n.*1483T>A
ENST00000579314.5:c.*1457T>A	ENSP00000462599.1:n.*1457T>A
NM_000789.3:c.3728T>A	NP_000780.1:p.Val1243Asp
NM_001178057.1:c.1883T>A	NP_001171528.1:p.Val628Asp
NM_152830.2:c.2006T>A	NP_690043.1:p.Val669Asp
XM_005257110.1:c.3179T>A	XP_005257167.1:p.Val1060Asp
XM_006721737.2:c.2066T>A	XP_006721800.2:p.Val689Asp
XM_006721737.3:c.2066T>A	XP_006721800.2:p.Val689Asp
NM_000789.4:c.3728T>A MANE Select	NP_000780.1:p.Val1243Asp
NM_001178057.2:c.1883T>A	NP_001171528.1:p.Val628Asp
NM_152830.3:c.2006T>A	NP_690043.1:p.Val669Asp
NM_001382700.1:c.3161T>A	NP_001369629.1:p.Val1054Asp
NM_001382701.1:c.2876T>A	NP_001369630.1:p.Val959Asp
NM_001382702.1:c.1343T>A	NP_001369631.1:p.Val448Asp
NR_168483.1:n.2106T>A