Canonical Allele Identifier: CA400556719

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564377A>T (hg19) ; chr17:g.63487016A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487016A>T , CM000679.2:g.63487016A>T	GRCh38
NC_000017.10:g.61564377A>T , CM000679.1:g.61564377A>T	GRCh37
NC_000017.9:g.58918109A>T	NCBI36
NG_011648.1:g.14944A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2248A>T MANE Select	ENSP00000290866.4:p.Thr750Ser
ENST00000290863.10:c.526A>T	ENSP00000290863.6:p.Thr176Ser
ENST00000290866.9:c.2248A>T	ENSP00000290866.4:p.Thr750Ser
ENST00000413513.7:c.526A>T	ENSP00000392247.3:p.Thr176Ser
ENST00000428043.5:c.2248A>T	ENSP00000397593.2:p.Thr750Ser
ENST00000577647.2:c.526A>T	ENSP00000464149.1:p.Thr176Ser
ENST00000578839.5:c.*318A>T	ENSP00000462110.2:n.*318A>T
ENST00000579204.1:c.429A>T	ENSP00000464629.1:n.429A>T
ENST00000579314.5:c.526A>T	ENSP00000462599.1:p.Thr176Ser
ENST00000579726.5:c.810A>T
ENST00000582005.5:c.*168A>T	ENSP00000462002.1:n.*168A>T
ENST00000582761.1:c.16A>T	ENSP00000462909.1:p.Thr6Ser
ENST00000584865.5:n.194A>T
NM_000789.3:c.2248A>T	NP_000780.1:p.Thr750Ser
NM_001178057.1:c.526A>T	NP_001171528.1:p.Thr176Ser
NM_152830.2:c.526A>T	NP_690043.1:p.Thr176Ser
XM_005257110.1:c.1699A>T	XP_005257167.1:p.Thr567Ser
XM_006721737.2:c.586A>T	XP_006721800.2:p.Thr196Ser
XM_006721737.3:c.586A>T	XP_006721800.2:p.Thr196Ser
NM_000789.4:c.2248A>T MANE Select	NP_000780.1:p.Thr750Ser
NM_001178057.2:c.526A>T	NP_001171528.1:p.Thr176Ser
NM_152830.3:c.526A>T	NP_690043.1:p.Thr176Ser
NM_001382700.1:c.1681A>T	NP_001369629.1:p.Thr561Ser
NM_001382701.1:c.1396A>T	NP_001369630.1:p.Thr466Ser
NM_001382702.1:c.178A>T	NP_001369631.1:p.Thr60Ser
NR_168483.1:n.548A>T