Canonical Allele Identifier: CA400569170

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574647T>G (hg19) ; chr17:g.63497286T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497286T>G , CM000679.2:g.63497286T>G	GRCh38
NC_000017.10:g.61574647T>G , CM000679.1:g.61574647T>G	GRCh37
NC_000017.9:g.58928379T>G	NCBI36
NG_011648.1:g.25214T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3841T>G MANE Select	ENSP00000290866.4:p.Phe1281Val
ENST00000290863.10:c.2119T>G	ENSP00000290863.6:p.Phe707Val
ENST00000290866.9:c.3841T>G	ENSP00000290866.4:p.Phe1281Val
ENST00000413513.7:c.1996T>G	ENSP00000392247.3:p.Phe666Val
ENST00000428043.5:c.*263T>G	ENSP00000397593.2:n.*263T>G
ENST00000577647.2:c.1969+301T>G	ENSP00000464149.1:n.1969+301T>G
ENST00000578839.5:c.*1596T>G	ENSP00000462110.2:n.*1596T>G
ENST00000579314.5:c.*1570T>G	ENSP00000462599.1:n.*1570T>G
NM_000789.3:c.3841T>G	NP_000780.1:p.Phe1281Val
NM_001178057.1:c.1996T>G	NP_001171528.1:p.Phe666Val
NM_152830.2:c.2119T>G	NP_690043.1:p.Phe707Val
XM_005257110.1:c.3292T>G	XP_005257167.1:p.Phe1098Val
XM_006721737.2:c.2179T>G	XP_006721800.2:p.Phe727Val
XM_006721737.3:c.2179T>G	XP_006721800.2:p.Phe727Val
NM_000789.4:c.3841T>G MANE Select	NP_000780.1:p.Phe1281Val
NM_001178057.2:c.1996T>G	NP_001171528.1:p.Phe666Val
NM_152830.3:c.2119T>G	NP_690043.1:p.Phe707Val
NM_001382700.1:c.3274T>G	NP_001369629.1:p.Phe1092Val
NM_001382701.1:c.2989T>G	NP_001369630.1:p.Phe997Val
NM_001382702.1:c.1456T>G	NP_001369631.1:p.Phe486Val
NR_168483.1:n.2219T>G