Canonical Allele Identifier: CA501341705

Gene: ACE

Linked Data

• dbSNP Id: rs903738622
• MyVariant Identifiers: chr17:g.61559929C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482568C>A , CM000679.2:g.63482568C>A	GRCh38
NC_000017.10:g.61559929C>A , CM000679.1:g.61559929C>A	GRCh37
NC_000017.9:g.58913661C>A	NCBI36
NG_011648.1:g.10496C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1221C>A MANE Select	ENSP00000290866.4:p.Ser407=
ENST00000290866.9:c.1221C>A	ENSP00000290866.4:p.Ser407=
ENST00000428043.5:c.1221C>A	ENSP00000397593.2:p.Ser407=
ENST00000582678.5:c.*620C>A	ENSP00000462995.1:n.*620C>A
ENST00000584529.5:n.1255C>A
NM_000789.3:c.1221C>A	NP_000780.1:p.Ser407=
XM_005257110.1:c.672C>A	XP_005257167.1:p.Ser224=
NM_000789.4:c.1221C>A MANE Select	NP_000780.1:p.Ser407=
NM_001382700.1:c.654C>A	NP_001369629.1:p.Ser218=
NM_001382701.1:c.369C>A	NP_001369630.1:p.Ser123=