Canonical Allele Identifier: CA400556982

Gene: ACE

Linked Data

• gnomAD v4: 17-63487073-G-A
• MyVariant Identifiers: chr17:g.61564434G>A (hg19) ; chr17:g.63487073G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487073G>A , CM000679.2:g.63487073G>A	GRCh38
NC_000017.10:g.61564434G>A , CM000679.1:g.61564434G>A	GRCh37
NC_000017.9:g.58918166G>A	NCBI36
NG_011648.1:g.15001G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2305G>A MANE Select	ENSP00000290866.4:p.Asp769Asn
ENST00000290863.10:c.583G>A	ENSP00000290863.6:p.Asp195Asn
ENST00000290866.9:c.2305G>A	ENSP00000290866.4:p.Asp769Asn
ENST00000413513.7:c.583G>A	ENSP00000392247.3:p.Asp195Asn
ENST00000428043.5:c.2305G>A	ENSP00000397593.2:p.Asp769Asn
ENST00000577647.2:c.583G>A	ENSP00000464149.1:p.Asp195Asn
ENST00000578839.5:c.*375G>A	ENSP00000462110.2:n.*375G>A
ENST00000579204.1:c.486G>A	ENSP00000464629.1:n.486G>A
ENST00000579314.5:c.583G>A	ENSP00000462599.1:p.Ala195Thr
ENST00000579726.5:c.867G>A
ENST00000582005.5:c.*225G>A	ENSP00000462002.1:n.*225G>A
ENST00000582761.1:c.73G>A	ENSP00000462909.1:p.Asp25Asn
ENST00000584865.5:n.251G>A
NM_000789.3:c.2305G>A	NP_000780.1:p.Asp769Asn
NM_001178057.1:c.583G>A	NP_001171528.1:p.Asp195Asn
NM_152830.2:c.583G>A	NP_690043.1:p.Asp195Asn
XM_005257110.1:c.1756G>A	XP_005257167.1:p.Asp586Asn
XM_006721737.2:c.643G>A	XP_006721800.2:p.Asp215Asn
XM_006721737.3:c.643G>A	XP_006721800.2:p.Asp215Asn
NM_000789.4:c.2305G>A MANE Select	NP_000780.1:p.Asp769Asn
NM_001178057.2:c.583G>A	NP_001171528.1:p.Asp195Asn
NM_152830.3:c.583G>A	NP_690043.1:p.Asp195Asn
NM_001382700.1:c.1738G>A	NP_001369629.1:p.Asp580Asn
NM_001382701.1:c.1453G>A	NP_001369630.1:p.Asp485Asn
NM_001382702.1:c.235G>A	NP_001369631.1:p.Asp79Asn
NR_168483.1:n.605G>A