Canonical Allele Identifier: CA400540740

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61555371A>T (hg19) ; chr17:g.63478010A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478010A>T , CM000679.2:g.63478010A>T	GRCh38
NC_000017.10:g.61555371A>T , CM000679.1:g.61555371A>T	GRCh37
NC_000017.9:g.58909103A>T	NCBI36
NG_011648.1:g.5938A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.329A>T MANE Select	ENSP00000290866.4:p.Gln110Leu
ENST00000290866.9:c.329A>T	ENSP00000290866.4:p.Gln110Leu
ENST00000428043.5:c.329A>T	ENSP00000397593.2:p.Gln110Leu
ENST00000579462.1:n.354A>T
ENST00000580318.1:n.518A>T
ENST00000582627.1:c.329A>T	ENSP00000462280.1:p.Gln110Leu
ENST00000582678.5:c.329A>T	ENSP00000462995.1:p.Gln110Leu
ENST00000583336.5:n.363A>T
ENST00000584529.5:n.363A>T
NM_000789.3:c.329A>T	NP_000780.1:p.Gln110Leu
XM_005257110.1:c.-127A>T	XP_005257167.1:n.-127A>T
NM_000789.4:c.329A>T MANE Select	NP_000780.1:p.Gln110Leu
NM_001382700.1:c.94A>T	NP_001369629.1:p.Arg32Ter
NM_001382701.1:c.-286A>T	NP_001369630.1:n.-286A>T