Canonical Allele Identifier: CA501341466

Gene: ACE

Linked Data

• gnomAD v4: 17-63477975-C-T
• MyVariant Identifiers: chr17:g.61555336C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477975C>T , CM000679.2:g.63477975C>T	GRCh38
NC_000017.10:g.61555336C>T , CM000679.1:g.61555336C>T	GRCh37
NC_000017.9:g.58909068C>T	NCBI36
NG_011648.1:g.5903C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.294C>T MANE Select	ENSP00000290866.4:p.Gly98=
ENST00000290866.9:c.294C>T	ENSP00000290866.4:p.Gly98=
ENST00000428043.5:c.294C>T	ENSP00000397593.2:p.Gly98=
ENST00000579462.1:n.319C>T
ENST00000580318.1:n.483C>T
ENST00000582627.1:c.294C>T	ENSP00000462280.1:p.Gly98=
ENST00000582678.5:c.294C>T	ENSP00000462995.1:p.Gly98=
ENST00000583336.5:n.328C>T
ENST00000584529.5:n.328C>T
NM_000789.3:c.294C>T	NP_000780.1:p.Gly98=
XM_005257110.1:c.-162C>T	XP_005257167.1:n.-162C>T
NM_000789.4:c.294C>T MANE Select	NP_000780.1:p.Gly98=
NM_001382700.1:c.59C>T	NP_001369629.1:p.Ala20Val
NM_001382701.1:c.-321C>T	NP_001369630.1:n.-321C>T