Canonical Allele Identifier: CA400569422

Gene: ACE

Linked Data

• gnomAD v4: 17-63497310-C-T
• MyVariant Identifiers: chr17:g.61574671C>T (hg19) ; chr17:g.63497310C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497310C>T , CM000679.2:g.63497310C>T	GRCh38
NC_000017.10:g.61574671C>T , CM000679.1:g.61574671C>T	GRCh37
NC_000017.9:g.58928403C>T	NCBI36
NG_011648.1:g.25238C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3865C>T MANE Select	ENSP00000290866.4:p.His1289Tyr
ENST00000290863.10:c.2143C>T	ENSP00000290863.6:p.His715Tyr
ENST00000290866.9:c.3865C>T	ENSP00000290866.4:p.His1289Tyr
ENST00000413513.7:c.2020C>T	ENSP00000392247.3:p.His674Tyr
ENST00000428043.5:c.*287C>T	ENSP00000397593.2:n.*287C>T
ENST00000577647.2:c.1969+325C>T	ENSP00000464149.1:n.1969+325C>T
ENST00000578839.5:c.*1620C>T	ENSP00000462110.2:n.*1620C>T
ENST00000579314.5:c.*1594C>T	ENSP00000462599.1:n.*1594C>T
NM_000789.3:c.3865C>T	NP_000780.1:p.His1289Tyr
NM_001178057.1:c.2020C>T	NP_001171528.1:p.His674Tyr
NM_152830.2:c.2143C>T	NP_690043.1:p.His715Tyr
XM_005257110.1:c.3316C>T	XP_005257167.1:p.His1106Tyr
XM_006721737.2:c.2203C>T	XP_006721800.2:p.His735Tyr
XM_006721737.3:c.2203C>T	XP_006721800.2:p.His735Tyr
NM_000789.4:c.3865C>T MANE Select	NP_000780.1:p.His1289Tyr
NM_001178057.2:c.2020C>T	NP_001171528.1:p.His674Tyr
NM_152830.3:c.2143C>T	NP_690043.1:p.His715Tyr
NM_001382700.1:c.3298C>T	NP_001369629.1:p.His1100Tyr
NM_001382701.1:c.3013C>T	NP_001369630.1:p.His1005Tyr
NM_001382702.1:c.1480C>T	NP_001369631.1:p.His494Tyr
NR_168483.1:n.2243C>T