Canonical Allele Identifier: CA400556795

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564392A>T (hg19) ; chr17:g.63487031A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487031A>T , CM000679.2:g.63487031A>T	GRCh38
NC_000017.10:g.61564392A>T , CM000679.1:g.61564392A>T	GRCh37
NC_000017.9:g.58918124A>T	NCBI36
NG_011648.1:g.14959A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2263A>T MANE Select	ENSP00000290866.4:p.Thr755Ser
ENST00000290863.10:c.541A>T	ENSP00000290863.6:p.Thr181Ser
ENST00000290866.9:c.2263A>T	ENSP00000290866.4:p.Thr755Ser
ENST00000413513.7:c.541A>T	ENSP00000392247.3:p.Thr181Ser
ENST00000428043.5:c.2263A>T	ENSP00000397593.2:p.Thr755Ser
ENST00000577647.2:c.541A>T	ENSP00000464149.1:p.Thr181Ser
ENST00000578839.5:c.*333A>T	ENSP00000462110.2:n.*333A>T
ENST00000579204.1:c.444A>T	ENSP00000464629.1:n.444A>T
ENST00000579314.5:c.541A>T	ENSP00000462599.1:p.Thr181Ser
ENST00000579726.5:c.825A>T
ENST00000582005.5:c.*183A>T	ENSP00000462002.1:n.*183A>T
ENST00000582761.1:c.31A>T	ENSP00000462909.1:p.Thr11Ser
ENST00000584865.5:n.209A>T
NM_000789.3:c.2263A>T	NP_000780.1:p.Thr755Ser
NM_001178057.1:c.541A>T	NP_001171528.1:p.Thr181Ser
NM_152830.2:c.541A>T	NP_690043.1:p.Thr181Ser
XM_005257110.1:c.1714A>T	XP_005257167.1:p.Thr572Ser
XM_006721737.2:c.601A>T	XP_006721800.2:p.Thr201Ser
XM_006721737.3:c.601A>T	XP_006721800.2:p.Thr201Ser
NM_000789.4:c.2263A>T MANE Select	NP_000780.1:p.Thr755Ser
NM_001178057.2:c.541A>T	NP_001171528.1:p.Thr181Ser
NM_152830.3:c.541A>T	NP_690043.1:p.Thr181Ser
NM_001382700.1:c.1696A>T	NP_001369629.1:p.Thr566Ser
NM_001382701.1:c.1411A>T	NP_001369630.1:p.Thr471Ser
NM_001382702.1:c.193A>T	NP_001369631.1:p.Thr65Ser
NR_168483.1:n.563A>T