Canonical Allele Identifier: CA501341697

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61559923C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482562C>A , CM000679.2:g.63482562C>A	GRCh38
NC_000017.10:g.61559923C>A , CM000679.1:g.61559923C>A	GRCh37
NC_000017.9:g.58913655C>A	NCBI36
NG_011648.1:g.10490C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1215C>A MANE Select	ENSP00000290866.4:p.Pro405=
ENST00000290866.9:c.1215C>A	ENSP00000290866.4:p.Pro405=
ENST00000428043.5:c.1215C>A	ENSP00000397593.2:p.Pro405=
ENST00000582678.5:c.*614C>A	ENSP00000462995.1:n.*614C>A
ENST00000584529.5:n.1249C>A
NM_000789.3:c.1215C>A	NP_000780.1:p.Pro405=
XM_005257110.1:c.666C>A	XP_005257167.1:p.Pro222=
NM_000789.4:c.1215C>A MANE Select	NP_000780.1:p.Pro405=
NM_001382700.1:c.648C>A	NP_001369629.1:p.Pro216=
NM_001382701.1:c.363C>A	NP_001369630.1:p.Pro121=