Canonical Allele Identifier: CA501341613

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61559845G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482484G>T , CM000679.2:g.63482484G>T	GRCh38
NC_000017.10:g.61559845G>T , CM000679.1:g.61559845G>T	GRCh37
NC_000017.9:g.58913577G>T	NCBI36
NG_011648.1:g.10412G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1137G>T MANE Select	ENSP00000290866.4:p.Arg379=
ENST00000290866.9:c.1137G>T	ENSP00000290866.4:p.Arg379=
ENST00000428043.5:c.1137G>T	ENSP00000397593.2:p.Arg379=
ENST00000582678.5:c.*536G>T	ENSP00000462995.1:n.*536G>T
ENST00000584529.5:n.1171G>T
NM_000789.3:c.1137G>T	NP_000780.1:p.Arg379=
XM_005257110.1:c.588G>T	XP_005257167.1:p.Arg196=
NM_000789.4:c.1137G>T MANE Select	NP_000780.1:p.Arg379=
NM_001382700.1:c.570G>T	NP_001369629.1:p.Arg190=
NM_001382701.1:c.285G>T	NP_001369630.1:p.Arg95=