Canonical Allele Identifier: CA400540875

Gene: ACE

Linked Data

• gnomAD v4: 17-63478078-C-T
• MyVariant Identifiers: chr17:g.61555439C>T (hg19) ; chr17:g.63478078C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478078C>T , CM000679.2:g.63478078C>T	GRCh38
NC_000017.10:g.61555439C>T , CM000679.1:g.61555439C>T	GRCh37
NC_000017.9:g.58909171C>T	NCBI36
NG_011648.1:g.6006C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.397C>T MANE Select	ENSP00000290866.4:p.Pro133Ser
ENST00000290866.9:c.397C>T	ENSP00000290866.4:p.Pro133Ser
ENST00000428043.5:c.397C>T	ENSP00000397593.2:p.Pro133Ser
ENST00000579462.1:n.422C>T
ENST00000580318.1:n.586C>T
ENST00000582627.1:c.397C>T	ENSP00000462280.1:p.Pro133Ser
ENST00000582678.5:c.397C>T	ENSP00000462995.1:p.Pro133Ser
ENST00000583336.5:n.431C>T
ENST00000584529.5:n.431C>T
NM_000789.3:c.397C>T	NP_000780.1:p.Pro133Ser
XM_005257110.1:c.-59C>T	XP_005257167.1:n.-59C>T
NM_000789.4:c.397C>T MANE Select	NP_000780.1:p.Pro133Ser
NM_001382700.1:c.162C>T	NP_001369629.1:p.Cys54=
NM_001382701.1:c.-218C>T	NP_001369630.1:n.-218C>T