Canonical Allele Identifier: CA400558560

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566411T>A (hg19) ; chr17:g.63489050T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63489050T>A , CM000679.2:g.63489050T>A	GRCh38
NC_000017.10:g.61566411T>A , CM000679.1:g.61566411T>A	GRCh37
NC_000017.9:g.58920143T>A	NCBI36
NG_011648.1:g.16978T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2559T>A MANE Select	ENSP00000290866.4:p.His853Gln
ENST00000290863.10:c.837T>A	ENSP00000290863.6:p.His279Gln
ENST00000290866.9:c.2559T>A	ENSP00000290866.4:p.His853Gln
ENST00000413513.7:c.837T>A	ENSP00000392247.3:p.His279Gln
ENST00000428043.5:c.2559T>A	ENSP00000397593.2:p.His853Gln
ENST00000577647.2:c.837T>A	ENSP00000464149.1:p.His279Gln
ENST00000578839.5:c.*519+259T>A	ENSP00000462110.2:n.*519+259T>A
ENST00000579314.5:c.*288T>A	ENSP00000462599.1:n.*288T>A
ENST00000582005.5:c.*479T>A	ENSP00000462002.1:n.*479T>A
ENST00000582761.1:c.327T>A	ENSP00000462909.1:p.His109Gln
ENST00000584865.5:n.505T>A
NM_000789.3:c.2559T>A	NP_000780.1:p.His853Gln
NM_001178057.1:c.837T>A	NP_001171528.1:p.His279Gln
NM_152830.2:c.837T>A	NP_690043.1:p.His279Gln
XM_005257110.1:c.2010T>A	XP_005257167.1:p.His670Gln
XM_006721737.2:c.897T>A	XP_006721800.2:p.His299Gln
XM_006721737.3:c.897T>A	XP_006721800.2:p.His299Gln
NM_000789.4:c.2559T>A MANE Select	NP_000780.1:p.His853Gln
NM_001178057.2:c.837T>A	NP_001171528.1:p.His279Gln
NM_152830.3:c.837T>A	NP_690043.1:p.His279Gln
NM_001382700.1:c.1992T>A	NP_001369629.1:p.His664Gln
NM_001382701.1:c.1707T>A	NP_001369630.1:p.His569Gln
NM_001382702.1:c.379+259T>A	NP_001369631.1:n.379+259T>A
NR_168483.1:n.937T>A