Canonical Allele Identifier: CA400556928

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564422C>A (hg19) ; chr17:g.63487061C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487061C>A , CM000679.2:g.63487061C>A	GRCh38
NC_000017.10:g.61564422C>A , CM000679.1:g.61564422C>A	GRCh37
NC_000017.9:g.58918154C>A	NCBI36
NG_011648.1:g.14989C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2293C>A MANE Select	ENSP00000290866.4:p.Gln765Lys
ENST00000290863.10:c.571C>A	ENSP00000290863.6:p.Gln191Lys
ENST00000290866.9:c.2293C>A	ENSP00000290866.4:p.Gln765Lys
ENST00000413513.7:c.571C>A	ENSP00000392247.3:p.Gln191Lys
ENST00000428043.5:c.2293C>A	ENSP00000397593.2:p.Gln765Lys
ENST00000577647.2:c.571C>A	ENSP00000464149.1:p.Gln191Lys
ENST00000578839.5:c.*363C>A	ENSP00000462110.2:n.*363C>A
ENST00000579204.1:c.474C>A	ENSP00000464629.1:n.474C>A
ENST00000579314.5:c.571C>A	ENSP00000462599.1:p.Gln191Lys
ENST00000579726.5:c.855C>A
ENST00000582005.5:c.*213C>A	ENSP00000462002.1:n.*213C>A
ENST00000582761.1:c.61C>A	ENSP00000462909.1:p.Gln21Lys
ENST00000584865.5:n.239C>A
NM_000789.3:c.2293C>A	NP_000780.1:p.Gln765Lys
NM_001178057.1:c.571C>A	NP_001171528.1:p.Gln191Lys
NM_152830.2:c.571C>A	NP_690043.1:p.Gln191Lys
XM_005257110.1:c.1744C>A	XP_005257167.1:p.Gln582Lys
XM_006721737.2:c.631C>A	XP_006721800.2:p.Gln211Lys
XM_006721737.3:c.631C>A	XP_006721800.2:p.Gln211Lys
NM_000789.4:c.2293C>A MANE Select	NP_000780.1:p.Gln765Lys
NM_001178057.2:c.571C>A	NP_001171528.1:p.Gln191Lys
NM_152830.3:c.571C>A	NP_690043.1:p.Gln191Lys
NM_001382700.1:c.1726C>A	NP_001369629.1:p.Gln576Lys
NM_001382701.1:c.1441C>A	NP_001369630.1:p.Gln481Lys
NM_001382702.1:c.223C>A	NP_001369631.1:p.Gln75Lys
NR_168483.1:n.593C>A