Canonical Allele Identifier: CA400558155

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566319G>T (hg19) ; chr17:g.63488958G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488958G>T , CM000679.2:g.63488958G>T	GRCh38
NC_000017.10:g.61566319G>T , CM000679.1:g.61566319G>T	GRCh37
NC_000017.9:g.58920051G>T	NCBI36
NG_011648.1:g.16886G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2467G>T MANE Select	ENSP00000290866.4:p.Asp823Tyr
ENST00000290863.10:c.745G>T	ENSP00000290863.6:p.Asp249Tyr
ENST00000290866.9:c.2467G>T	ENSP00000290866.4:p.Asp823Tyr
ENST00000413513.7:c.745G>T	ENSP00000392247.3:p.Asp249Tyr
ENST00000428043.5:c.2467G>T	ENSP00000397593.2:p.Asp823Tyr
ENST00000577647.2:c.745G>T	ENSP00000464149.1:p.Asp249Tyr
ENST00000578839.5:c.*519+167G>T	ENSP00000462110.2:n.*519+167G>T
ENST00000579204.1:c.726G>T	ENSP00000464629.1:n.726G>T
ENST00000579314.5:c.*196G>T	ENSP00000462599.1:n.*196G>T
ENST00000582005.5:c.*387G>T	ENSP00000462002.1:n.*387G>T
ENST00000582761.1:c.235G>T	ENSP00000462909.1:p.Asp79Tyr
ENST00000584865.5:n.413G>T
NM_000789.3:c.2467G>T	NP_000780.1:p.Asp823Tyr
NM_001178057.1:c.745G>T	NP_001171528.1:p.Asp249Tyr
NM_152830.2:c.745G>T	NP_690043.1:p.Asp249Tyr
XM_005257110.1:c.1918G>T	XP_005257167.1:p.Asp640Tyr
XM_006721737.2:c.805G>T	XP_006721800.2:p.Asp269Tyr
XM_006721737.3:c.805G>T	XP_006721800.2:p.Asp269Tyr
NM_000789.4:c.2467G>T MANE Select	NP_000780.1:p.Asp823Tyr
NM_001178057.2:c.745G>T	NP_001171528.1:p.Asp249Tyr
NM_152830.3:c.745G>T	NP_690043.1:p.Asp249Tyr
NM_001382700.1:c.1900G>T	NP_001369629.1:p.Asp634Tyr
NM_001382701.1:c.1615G>T	NP_001369630.1:p.Asp539Tyr
NM_001382702.1:c.379+167G>T	NP_001369631.1:n.379+167G>T
NR_168483.1:n.845G>T