Canonical Allele Identifier: CA400540586

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61555305T>G (hg19) ; chr17:g.63477944T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477944T>G , CM000679.2:g.63477944T>G	GRCh38
NC_000017.10:g.61555305T>G , CM000679.1:g.61555305T>G	GRCh37
NC_000017.9:g.58909037T>G	NCBI36
NG_011648.1:g.5872T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.263T>G MANE Select	ENSP00000290866.4:p.Leu88Arg
ENST00000290866.9:c.263T>G	ENSP00000290866.4:p.Leu88Arg
ENST00000428043.5:c.263T>G	ENSP00000397593.2:p.Leu88Arg
ENST00000579462.1:n.288T>G
ENST00000580318.1:n.452T>G
ENST00000582627.1:c.263T>G	ENSP00000462280.1:p.Leu88Arg
ENST00000582678.5:c.263T>G	ENSP00000462995.1:p.Leu88Arg
ENST00000583336.5:n.297T>G
ENST00000584529.5:n.297T>G
NM_000789.3:c.263T>G	NP_000780.1:p.Leu88Arg
XM_005257110.1:c.-193T>G	XP_005257167.1:n.-193T>G
NM_000789.4:c.263T>G MANE Select	NP_000780.1:p.Leu88Arg
NM_001382700.1:c.28T>G	NP_001369629.1:p.Cys10Gly
NM_001382701.1:c.-352T>G	NP_001369630.1:n.-352T>G