Canonical Allele Identifier: CA400568767

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574578G>C (hg19) ; chr17:g.63497217G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497217G>C , CM000679.2:g.63497217G>C	GRCh38
NC_000017.10:g.61574578G>C , CM000679.1:g.61574578G>C	GRCh37
NC_000017.9:g.58928310G>C	NCBI36
NG_011648.1:g.25145G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3772G>C MANE Select	ENSP00000290866.4:p.Gly1258Arg
ENST00000290863.10:c.2050G>C	ENSP00000290863.6:p.Gly684Arg
ENST00000290866.9:c.3772G>C	ENSP00000290866.4:p.Gly1258Arg
ENST00000413513.7:c.1927G>C	ENSP00000392247.3:p.Gly643Arg
ENST00000428043.5:c.*194G>C	ENSP00000397593.2:n.*194G>C
ENST00000577647.2:c.1969+232G>C	ENSP00000464149.1:n.1969+232G>C
ENST00000578839.5:c.*1527G>C	ENSP00000462110.2:n.*1527G>C
ENST00000579314.5:c.*1501G>C	ENSP00000462599.1:n.*1501G>C
NM_000789.3:c.3772G>C	NP_000780.1:p.Gly1258Arg
NM_001178057.1:c.1927G>C	NP_001171528.1:p.Gly643Arg
NM_152830.2:c.2050G>C	NP_690043.1:p.Gly684Arg
XM_005257110.1:c.3223G>C	XP_005257167.1:p.Gly1075Arg
XM_006721737.2:c.2110G>C	XP_006721800.2:p.Gly704Arg
XM_006721737.3:c.2110G>C	XP_006721800.2:p.Gly704Arg
NM_000789.4:c.3772G>C MANE Select	NP_000780.1:p.Gly1258Arg
NM_001178057.2:c.1927G>C	NP_001171528.1:p.Gly643Arg
NM_152830.3:c.2050G>C	NP_690043.1:p.Gly684Arg
NM_001382700.1:c.3205G>C	NP_001369629.1:p.Gly1069Arg
NM_001382701.1:c.2920G>C	NP_001369630.1:p.Gly974Arg
NM_001382702.1:c.1387G>C	NP_001369631.1:p.Gly463Arg
NR_168483.1:n.2150G>C