Canonical Allele Identifier: CA400540573

Gene: ACE

Linked Data

• dbSNP Id: rs1440389747
• MyVariant Identifiers: chr17:g.61555301G>T (hg19) ; chr17:g.63477940G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477940G>T , CM000679.2:g.63477940G>T	GRCh38
NC_000017.10:g.61555301G>T , CM000679.1:g.61555301G>T	GRCh37
NC_000017.9:g.58909033G>T	NCBI36
NG_011648.1:g.5868G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.259G>T MANE Select	ENSP00000290866.4:p.Ala87Ser
ENST00000290866.9:c.259G>T	ENSP00000290866.4:p.Ala87Ser
ENST00000428043.5:c.259G>T	ENSP00000397593.2:p.Ala87Ser
ENST00000579462.1:n.284G>T
ENST00000580318.1:n.448G>T
ENST00000582627.1:c.259G>T	ENSP00000462280.1:p.Ala87Ser
ENST00000582678.5:c.259G>T	ENSP00000462995.1:p.Ala87Ser
ENST00000583336.5:n.293G>T
ENST00000584529.5:n.293G>T
NM_000789.3:c.259G>T	NP_000780.1:p.Ala87Ser
XM_005257110.1:c.-197G>T	XP_005257167.1:n.-197G>T
NM_000789.4:c.259G>T MANE Select	NP_000780.1:p.Ala87Ser
NM_001382700.1:c.24G>T	NP_001369629.1:p.Gln8His
NM_001382701.1:c.-356G>T	NP_001369630.1:n.-356G>T