Canonical Allele Identifier: CA501341715

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61559935T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482574T>G , CM000679.2:g.63482574T>G	GRCh38
NC_000017.10:g.61559935T>G , CM000679.1:g.61559935T>G	GRCh37
NC_000017.9:g.58913667T>G	NCBI36
NG_011648.1:g.10502T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1227T>G MANE Select	ENSP00000290866.4:p.Arg409=
ENST00000290866.9:c.1227T>G	ENSP00000290866.4:p.Arg409=
ENST00000428043.5:c.1227T>G	ENSP00000397593.2:p.Arg409=
ENST00000582678.5:c.*626T>G	ENSP00000462995.1:n.*626T>G
ENST00000584529.5:n.1261T>G
NM_000789.3:c.1227T>G	NP_000780.1:p.Arg409=
XM_005257110.1:c.678T>G	XP_005257167.1:p.Arg226=
NM_000789.4:c.1227T>G MANE Select	NP_000780.1:p.Arg409=
NM_001382700.1:c.660T>G	NP_001369629.1:p.Arg220=
NM_001382701.1:c.375T>G	NP_001369630.1:p.Arg125=