Canonical Allele Identifier: CA400566632

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574181A>C (hg19) ; chr17:g.63496820A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496820A>C , CM000679.2:g.63496820A>C	GRCh38
NC_000017.10:g.61574181A>C , CM000679.1:g.61574181A>C	GRCh37
NC_000017.9:g.58927913A>C	NCBI36
NG_011648.1:g.24748A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3526A>C MANE Select	ENSP00000290866.4:p.Ser1176Arg
ENST00000290863.10:c.1804A>C	ENSP00000290863.6:p.Ser602Arg
ENST00000290866.9:c.3526A>C	ENSP00000290866.4:p.Ser1176Arg
ENST00000413513.7:c.1681A>C	ENSP00000392247.3:p.Ser561Arg
ENST00000428043.5:c.3526A>C	ENSP00000397593.2:p.Ser1176Arg
ENST00000577418.5:n.536A>C
ENST00000577647.2:c.1804A>C	ENSP00000464149.1:p.Ser602Arg
ENST00000578839.5:c.*1281A>C	ENSP00000462110.2:n.*1281A>C
ENST00000579314.5:c.*1255A>C	ENSP00000462599.1:n.*1255A>C
ENST00000579409.1:c.213A>C
ENST00000582244.1:n.400A>C
NM_000789.3:c.3526A>C	NP_000780.1:p.Ser1176Arg
NM_001178057.1:c.1681A>C	NP_001171528.1:p.Ser561Arg
NM_152830.2:c.1804A>C	NP_690043.1:p.Ser602Arg
XM_005257110.1:c.2977A>C	XP_005257167.1:p.Ser993Arg
XM_006721737.2:c.1864A>C	XP_006721800.2:p.Ser622Arg
XM_006721737.3:c.1864A>C	XP_006721800.2:p.Ser622Arg
NM_000789.4:c.3526A>C MANE Select	NP_000780.1:p.Ser1176Arg
NM_001178057.2:c.1681A>C	NP_001171528.1:p.Ser561Arg
NM_152830.3:c.1804A>C	NP_690043.1:p.Ser602Arg
NM_001382700.1:c.2959A>C	NP_001369629.1:p.Ser987Arg
NM_001382701.1:c.2674A>C	NP_001369630.1:p.Ser892Arg
NM_001382702.1:c.1141A>C	NP_001369631.1:p.Ser381Arg
NR_168483.1:n.1904A>C