Canonical Allele Identifier: CA400557901

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566063G>C (hg19) ; chr17:g.63488702G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488702G>C , CM000679.2:g.63488702G>C	GRCh38
NC_000017.10:g.61566063G>C , CM000679.1:g.61566063G>C	GRCh37
NC_000017.9:g.58919795G>C	NCBI36
NG_011648.1:g.16630G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2360G>C MANE Select	ENSP00000290866.4:p.Trp787Ser
ENST00000290863.10:c.638G>C	ENSP00000290863.6:p.Trp213Ser
ENST00000290866.9:c.2360G>C	ENSP00000290866.4:p.Trp787Ser
ENST00000413513.7:c.638G>C	ENSP00000392247.3:p.Trp213Ser
ENST00000428043.5:c.2360G>C	ENSP00000397593.2:p.Trp787Ser
ENST00000577647.2:c.638G>C	ENSP00000464149.1:p.Trp213Ser
ENST00000578839.5:c.*430G>C	ENSP00000462110.2:n.*430G>C
ENST00000579204.1:c.619G>C	ENSP00000464629.1:n.619G>C
ENST00000579314.5:c.*89G>C	ENSP00000462599.1:n.*89G>C
ENST00000582005.5:c.*280G>C	ENSP00000462002.1:n.*280G>C
ENST00000582761.1:c.128G>C	ENSP00000462909.1:p.Trp43Ser
ENST00000584865.5:n.306G>C
NM_000789.3:c.2360G>C	NP_000780.1:p.Trp787Ser
NM_001178057.1:c.638G>C	NP_001171528.1:p.Trp213Ser
NM_152830.2:c.638G>C	NP_690043.1:p.Trp213Ser
XM_005257110.1:c.1811G>C	XP_005257167.1:p.Trp604Ser
XM_006721737.2:c.698G>C	XP_006721800.2:p.Trp233Ser
XM_006721737.3:c.698G>C	XP_006721800.2:p.Trp233Ser
NM_000789.4:c.2360G>C MANE Select	NP_000780.1:p.Trp787Ser
NM_001178057.2:c.638G>C	NP_001171528.1:p.Trp213Ser
NM_152830.3:c.638G>C	NP_690043.1:p.Trp213Ser
NM_001382700.1:c.1793G>C	NP_001369629.1:p.Trp598Ser
NM_001382701.1:c.1508G>C	NP_001369630.1:p.Trp503Ser
NM_001382702.1:c.290G>C	NP_001369631.1:p.Trp97Ser
NR_168483.1:n.738G>C