Canonical Allele Identifier: CA400568913

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574605A>C (hg19) ; chr17:g.63497244A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497244A>C , CM000679.2:g.63497244A>C	GRCh38
NC_000017.10:g.61574605A>C , CM000679.1:g.61574605A>C	GRCh37
NC_000017.9:g.58928337A>C	NCBI36
NG_011648.1:g.25172A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3799A>C MANE Select	ENSP00000290866.4:p.Ile1267Leu
ENST00000290863.10:c.2077A>C	ENSP00000290863.6:p.Ile693Leu
ENST00000290866.9:c.3799A>C	ENSP00000290866.4:p.Ile1267Leu
ENST00000413513.7:c.1954A>C	ENSP00000392247.3:p.Ile652Leu
ENST00000428043.5:c.*221A>C	ENSP00000397593.2:n.*221A>C
ENST00000577647.2:c.1969+259A>C	ENSP00000464149.1:n.1969+259A>C
ENST00000578839.5:c.*1554A>C	ENSP00000462110.2:n.*1554A>C
ENST00000579314.5:c.*1528A>C	ENSP00000462599.1:n.*1528A>C
NM_000789.3:c.3799A>C	NP_000780.1:p.Ile1267Leu
NM_001178057.1:c.1954A>C	NP_001171528.1:p.Ile652Leu
NM_152830.2:c.2077A>C	NP_690043.1:p.Ile693Leu
XM_005257110.1:c.3250A>C	XP_005257167.1:p.Ile1084Leu
XM_006721737.2:c.2137A>C	XP_006721800.2:p.Ile713Leu
XM_006721737.3:c.2137A>C	XP_006721800.2:p.Ile713Leu
NM_000789.4:c.3799A>C MANE Select	NP_000780.1:p.Ile1267Leu
NM_001178057.2:c.1954A>C	NP_001171528.1:p.Ile652Leu
NM_152830.3:c.2077A>C	NP_690043.1:p.Ile693Leu
NM_001382700.1:c.3232A>C	NP_001369629.1:p.Ile1078Leu
NM_001382701.1:c.2947A>C	NP_001369630.1:p.Ile983Leu
NM_001382702.1:c.1414A>C	NP_001369631.1:p.Ile472Leu
NR_168483.1:n.2177A>C