Canonical Allele Identifier: CA400556835

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564402A>T (hg19) ; chr17:g.63487041A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487041A>T , CM000679.2:g.63487041A>T	GRCh38
NC_000017.10:g.61564402A>T , CM000679.1:g.61564402A>T	GRCh37
NC_000017.9:g.58918134A>T	NCBI36
NG_011648.1:g.14969A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2273A>T MANE Select	ENSP00000290866.4:p.His758Leu
ENST00000290863.10:c.551A>T	ENSP00000290863.6:p.His184Leu
ENST00000290866.9:c.2273A>T	ENSP00000290866.4:p.His758Leu
ENST00000413513.7:c.551A>T	ENSP00000392247.3:p.His184Leu
ENST00000428043.5:c.2273A>T	ENSP00000397593.2:p.His758Leu
ENST00000577647.2:c.551A>T	ENSP00000464149.1:p.His184Leu
ENST00000578839.5:c.*343A>T	ENSP00000462110.2:n.*343A>T
ENST00000579204.1:c.454A>T	ENSP00000464629.1:n.454A>T
ENST00000579314.5:c.551A>T	ENSP00000462599.1:p.His184Leu
ENST00000579726.5:c.835A>T
ENST00000582005.5:c.*193A>T	ENSP00000462002.1:n.*193A>T
ENST00000582761.1:c.41A>T	ENSP00000462909.1:p.His14Leu
ENST00000584865.5:n.219A>T
NM_000789.3:c.2273A>T	NP_000780.1:p.His758Leu
NM_001178057.1:c.551A>T	NP_001171528.1:p.His184Leu
NM_152830.2:c.551A>T	NP_690043.1:p.His184Leu
XM_005257110.1:c.1724A>T	XP_005257167.1:p.His575Leu
XM_006721737.2:c.611A>T	XP_006721800.2:p.His204Leu
XM_006721737.3:c.611A>T	XP_006721800.2:p.His204Leu
NM_000789.4:c.2273A>T MANE Select	NP_000780.1:p.His758Leu
NM_001178057.2:c.551A>T	NP_001171528.1:p.His184Leu
NM_152830.3:c.551A>T	NP_690043.1:p.His184Leu
NM_001382700.1:c.1706A>T	NP_001369629.1:p.His569Leu
NM_001382701.1:c.1421A>T	NP_001369630.1:p.His474Leu
NM_001382702.1:c.203A>T	NP_001369631.1:p.His68Leu
NR_168483.1:n.573A>T