Canonical Allele Identifier: CA400540644

Gene: ACE

Linked Data

• gnomAD v4: 17-63477970-T-C
• MyVariant Identifiers: chr17:g.61555331T>C (hg19) ; chr17:g.63477970T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477970T>C , CM000679.2:g.63477970T>C	GRCh38
NC_000017.10:g.61555331T>C , CM000679.1:g.61555331T>C	GRCh37
NC_000017.9:g.58909063T>C	NCBI36
NG_011648.1:g.5898T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.289T>C MANE Select	ENSP00000290866.4:p.Trp97Arg
ENST00000290866.9:c.289T>C	ENSP00000290866.4:p.Trp97Arg
ENST00000428043.5:c.289T>C	ENSP00000397593.2:p.Trp97Arg
ENST00000579462.1:n.314T>C
ENST00000580318.1:n.478T>C
ENST00000582627.1:c.289T>C	ENSP00000462280.1:p.Trp97Arg
ENST00000582678.5:c.289T>C	ENSP00000462995.1:p.Trp97Arg
ENST00000583336.5:n.323T>C
ENST00000584529.5:n.323T>C
NM_000789.3:c.289T>C	NP_000780.1:p.Trp97Arg
XM_005257110.1:c.-167T>C	XP_005257167.1:n.-167T>C
NM_000789.4:c.289T>C MANE Select	NP_000780.1:p.Trp97Arg
NM_001382700.1:c.54T>C	NP_001369629.1:p.Pro18=
NM_001382701.1:c.-326T>C	NP_001369630.1:n.-326T>C