Canonical Allele Identifier: CA400557887

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566057G>T (hg19) ; chr17:g.63488696G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488696G>T , CM000679.2:g.63488696G>T	GRCh38
NC_000017.10:g.61566057G>T , CM000679.1:g.61566057G>T	GRCh37
NC_000017.9:g.58919789G>T	NCBI36
NG_011648.1:g.16624G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2354G>T MANE Select	ENSP00000290866.4:p.Trp785Leu
ENST00000290863.10:c.632G>T	ENSP00000290863.6:p.Trp211Leu
ENST00000290866.9:c.2354G>T	ENSP00000290866.4:p.Trp785Leu
ENST00000413513.7:c.632G>T	ENSP00000392247.3:p.Trp211Leu
ENST00000428043.5:c.2354G>T	ENSP00000397593.2:p.Trp785Leu
ENST00000577647.2:c.632G>T	ENSP00000464149.1:p.Trp211Leu
ENST00000578839.5:c.*424G>T	ENSP00000462110.2:n.*424G>T
ENST00000579204.1:c.613G>T	ENSP00000464629.1:n.613G>T
ENST00000579314.5:c.*83G>T	ENSP00000462599.1:n.*83G>T
ENST00000582005.5:c.*274G>T	ENSP00000462002.1:n.*274G>T
ENST00000582761.1:c.122G>T	ENSP00000462909.1:p.Trp41Leu
ENST00000584865.5:n.300G>T
NM_000789.3:c.2354G>T	NP_000780.1:p.Trp785Leu
NM_001178057.1:c.632G>T	NP_001171528.1:p.Trp211Leu
NM_152830.2:c.632G>T	NP_690043.1:p.Trp211Leu
XM_005257110.1:c.1805G>T	XP_005257167.1:p.Trp602Leu
XM_006721737.2:c.692G>T	XP_006721800.2:p.Trp231Leu
XM_006721737.3:c.692G>T	XP_006721800.2:p.Trp231Leu
NM_000789.4:c.2354G>T MANE Select	NP_000780.1:p.Trp785Leu
NM_001178057.2:c.632G>T	NP_001171528.1:p.Trp211Leu
NM_152830.3:c.632G>T	NP_690043.1:p.Trp211Leu
NM_001382700.1:c.1787G>T	NP_001369629.1:p.Trp596Leu
NM_001382701.1:c.1502G>T	NP_001369630.1:p.Trp501Leu
NM_001382702.1:c.284G>T	NP_001369631.1:p.Trp95Leu
NR_168483.1:n.732G>T