Canonical Allele Identifier: CA501341403

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477283G>A , CM000679.2:g.63477283G>A	GRCh38
NC_000017.10:g.61554644G>A , CM000679.1:g.61554644G>A	GRCh37
NC_000017.9:g.58908376G>A	NCBI36
NG_011648.1:g.5211G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.189G>A MANE Select	ENSP00000290866.4:p.Gln63=
ENST00000290866.9:c.189G>A	ENSP00000290866.4:p.Gln63=
ENST00000428043.5:c.189G>A	ENSP00000397593.2:p.Gln63=
ENST00000579462.1:n.214G>A
ENST00000582678.5:c.189G>A	ENSP00000462995.1:p.Gln63=
ENST00000583336.5:n.223G>A
ENST00000584529.5:n.223G>A
NM_000789.3:c.189G>A	NP_000780.1:p.Gln63=
XM_005257110.1:c.-267G>A	XP_005257167.1:n.-267G>A
NM_000789.4:c.189G>A MANE Select	NP_000780.1:p.Gln63=
NM_001382700.1:c.-47G>A	NP_001369629.1:n.-47G>A
NM_001382701.1:c.-426G>A	NP_001369630.1:n.-426G>A