Canonical Allele Identifier: CA400556592

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564357T>A (hg19) ; chr17:g.63486996T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486996T>A , CM000679.2:g.63486996T>A	GRCh38
NC_000017.10:g.61564357T>A , CM000679.1:g.61564357T>A	GRCh37
NC_000017.9:g.58918089T>A	NCBI36
NG_011648.1:g.14924T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2228T>A MANE Select	ENSP00000290866.4:p.Ile743Asn
ENST00000290863.10:c.506T>A	ENSP00000290863.6:p.Ile169Asn
ENST00000290866.9:c.2228T>A	ENSP00000290866.4:p.Ile743Asn
ENST00000413513.7:c.506T>A	ENSP00000392247.3:p.Ile169Asn
ENST00000428043.5:c.2228T>A	ENSP00000397593.2:p.Ile743Asn
ENST00000577647.2:c.506T>A	ENSP00000464149.1:p.Ile169Asn
ENST00000578839.5:c.*298T>A	ENSP00000462110.2:n.*298T>A
ENST00000579204.1:c.409T>A	ENSP00000464629.1:n.409T>A
ENST00000579314.5:c.506T>A	ENSP00000462599.1:p.Ile169Asn
ENST00000579726.5:c.790T>A
ENST00000582005.5:c.*148T>A	ENSP00000462002.1:n.*148T>A
ENST00000584865.5:n.174T>A
NM_000789.3:c.2228T>A	NP_000780.1:p.Ile743Asn
NM_001178057.1:c.506T>A	NP_001171528.1:p.Ile169Asn
NM_152830.2:c.506T>A	NP_690043.1:p.Ile169Asn
XM_005257110.1:c.1679T>A	XP_005257167.1:p.Ile560Asn
XM_006721737.2:c.566T>A	XP_006721800.2:p.Ile189Asn
XM_006721737.3:c.566T>A	XP_006721800.2:p.Ile189Asn
NM_000789.4:c.2228T>A MANE Select	NP_000780.1:p.Ile743Asn
NM_001178057.2:c.506T>A	NP_001171528.1:p.Ile169Asn
NM_152830.3:c.506T>A	NP_690043.1:p.Ile169Asn
NM_001382700.1:c.1661T>A	NP_001369629.1:p.Ile554Asn
NM_001382701.1:c.1376T>A	NP_001369630.1:p.Ile459Asn
NM_001382702.1:c.158T>A	NP_001369631.1:p.Ile53Asn
NR_168483.1:n.528T>A