Canonical Allele Identifier: CA400540784

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61555390G>T (hg19) ; chr17:g.63478029G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478029G>T , CM000679.2:g.63478029G>T	GRCh38
NC_000017.10:g.61555390G>T , CM000679.1:g.61555390G>T	GRCh37
NC_000017.9:g.58909122G>T	NCBI36
NG_011648.1:g.5957G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.348G>T MANE Select	ENSP00000290866.4:p.Gln116His
ENST00000290866.9:c.348G>T	ENSP00000290866.4:p.Gln116His
ENST00000428043.5:c.348G>T	ENSP00000397593.2:p.Gln116His
ENST00000579462.1:n.373G>T
ENST00000580318.1:n.537G>T
ENST00000582627.1:c.348G>T	ENSP00000462280.1:p.Gln116His
ENST00000582678.5:c.348G>T	ENSP00000462995.1:p.Gln116His
ENST00000583336.5:n.382G>T
ENST00000584529.5:n.382G>T
NM_000789.3:c.348G>T	NP_000780.1:p.Gln116His
XM_005257110.1:c.-108G>T	XP_005257167.1:n.-108G>T
NM_000789.4:c.348G>T MANE Select	NP_000780.1:p.Gln116His
NM_001382700.1:c.113G>T	NP_001369629.1:p.Ser38Ile
NM_001382701.1:c.-267G>T	NP_001369630.1:n.-267G>T