Canonical Allele Identifier: CA501342329

Gene: ACE

Linked Data

• gnomAD v4: 17-63497210-C-T
• MyVariant Identifiers: chr17:g.61574571C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497210C>T , CM000679.2:g.63497210C>T	GRCh38
NC_000017.10:g.61574571C>T , CM000679.1:g.61574571C>T	GRCh37
NC_000017.9:g.58928303C>T	NCBI36
NG_011648.1:g.25138C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3765C>T MANE Select	ENSP00000290866.4:p.Ala1255=
ENST00000290863.10:c.2043C>T	ENSP00000290863.6:p.Ala681=
ENST00000290866.9:c.3765C>T	ENSP00000290866.4:p.Ala1255=
ENST00000413513.7:c.1920C>T	ENSP00000392247.3:p.Ala640=
ENST00000428043.5:c.*187C>T	ENSP00000397593.2:n.*187C>T
ENST00000577647.2:c.1969+225C>T	ENSP00000464149.1:n.1969+225C>T
ENST00000578839.5:c.*1520C>T	ENSP00000462110.2:n.*1520C>T
ENST00000579314.5:c.*1494C>T	ENSP00000462599.1:n.*1494C>T
NM_000789.3:c.3765C>T	NP_000780.1:p.Ala1255=
NM_001178057.1:c.1920C>T	NP_001171528.1:p.Ala640=
NM_152830.2:c.2043C>T	NP_690043.1:p.Ala681=
XM_005257110.1:c.3216C>T	XP_005257167.1:p.Ala1072=
XM_006721737.2:c.2103C>T	XP_006721800.2:p.Ala701=
XM_006721737.3:c.2103C>T	XP_006721800.2:p.Ala701=
NM_000789.4:c.3765C>T MANE Select	NP_000780.1:p.Ala1255=
NM_001178057.2:c.1920C>T	NP_001171528.1:p.Ala640=
NM_152830.3:c.2043C>T	NP_690043.1:p.Ala681=
NM_001382700.1:c.3198C>T	NP_001369629.1:p.Ala1066=
NM_001382701.1:c.2913C>T	NP_001369630.1:p.Ala971=
NM_001382702.1:c.1380C>T	NP_001369631.1:p.Ala460=
NR_168483.1:n.2143C>T