Canonical Allele Identifier: CA501188018

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566393A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63489032A>T , CM000679.2:g.63489032A>T	GRCh38
NC_000017.10:g.61566393A>T , CM000679.1:g.61566393A>T	GRCh37
NC_000017.9:g.58920125A>T	NCBI36
NG_011648.1:g.16960A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2541A>T MANE Select	ENSP00000290866.4:p.Pro847=
ENST00000290863.10:c.819A>T	ENSP00000290863.6:p.Pro273=
ENST00000290866.9:c.2541A>T	ENSP00000290866.4:p.Pro847=
ENST00000413513.7:c.819A>T	ENSP00000392247.3:p.Pro273=
ENST00000428043.5:c.2541A>T	ENSP00000397593.2:p.Pro847=
ENST00000577647.2:c.819A>T	ENSP00000464149.1:p.Pro273=
ENST00000578839.5:c.*519+241A>T	ENSP00000462110.2:n.*519+241A>T
ENST00000579204.1:c.800A>T	ENSP00000464629.1:n.800A>T
ENST00000579314.5:c.*270A>T	ENSP00000462599.1:n.*270A>T
ENST00000582005.5:c.*461A>T	ENSP00000462002.1:n.*461A>T
ENST00000582761.1:c.309A>T	ENSP00000462909.1:p.Pro103=
ENST00000584865.5:n.487A>T
NM_000789.3:c.2541A>T	NP_000780.1:p.Pro847=
NM_001178057.1:c.819A>T	NP_001171528.1:p.Pro273=
NM_152830.2:c.819A>T	NP_690043.1:p.Pro273=
XM_005257110.1:c.1992A>T	XP_005257167.1:p.Pro664=
XM_006721737.2:c.879A>T	XP_006721800.2:p.Pro293=
XM_006721737.3:c.879A>T	XP_006721800.2:p.Pro293=
NM_000789.4:c.2541A>T MANE Select	NP_000780.1:p.Pro847=
NM_001178057.2:c.819A>T	NP_001171528.1:p.Pro273=
NM_152830.3:c.819A>T	NP_690043.1:p.Pro273=
NM_001382700.1:c.1974A>T	NP_001369629.1:p.Pro658=
NM_001382701.1:c.1689A>T	NP_001369630.1:p.Pro563=
NM_001382702.1:c.379+241A>T	NP_001369631.1:n.379+241A>T
NR_168483.1:n.919A>T