Canonical Allele Identifier: CA400568760

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574576T>G (hg19) ; chr17:g.63497215T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497215T>G , CM000679.2:g.63497215T>G	GRCh38
NC_000017.10:g.61574576T>G , CM000679.1:g.61574576T>G	GRCh37
NC_000017.9:g.58928308T>G	NCBI36
NG_011648.1:g.25143T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3770T>G MANE Select	ENSP00000290866.4:p.Val1257Gly
ENST00000290863.10:c.2048T>G	ENSP00000290863.6:p.Val683Gly
ENST00000290866.9:c.3770T>G	ENSP00000290866.4:p.Val1257Gly
ENST00000413513.7:c.1925T>G	ENSP00000392247.3:p.Val642Gly
ENST00000428043.5:c.*192T>G	ENSP00000397593.2:n.*192T>G
ENST00000577647.2:c.1969+230T>G	ENSP00000464149.1:n.1969+230T>G
ENST00000578839.5:c.*1525T>G	ENSP00000462110.2:n.*1525T>G
ENST00000579314.5:c.*1499T>G	ENSP00000462599.1:n.*1499T>G
NM_000789.3:c.3770T>G	NP_000780.1:p.Val1257Gly
NM_001178057.1:c.1925T>G	NP_001171528.1:p.Val642Gly
NM_152830.2:c.2048T>G	NP_690043.1:p.Val683Gly
XM_005257110.1:c.3221T>G	XP_005257167.1:p.Val1074Gly
XM_006721737.2:c.2108T>G	XP_006721800.2:p.Val703Gly
XM_006721737.3:c.2108T>G	XP_006721800.2:p.Val703Gly
NM_000789.4:c.3770T>G MANE Select	NP_000780.1:p.Val1257Gly
NM_001178057.2:c.1925T>G	NP_001171528.1:p.Val642Gly
NM_152830.3:c.2048T>G	NP_690043.1:p.Val683Gly
NM_001382700.1:c.3203T>G	NP_001369629.1:p.Val1068Gly
NM_001382701.1:c.2918T>G	NP_001369630.1:p.Val973Gly
NM_001382702.1:c.1385T>G	NP_001369631.1:p.Val462Gly
NR_168483.1:n.2148T>G