Canonical Allele Identifier: CA400538255

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477119G>C , CM000679.2:g.63477119G>C	GRCh38
NC_000017.10:g.61554480G>C , CM000679.1:g.61554480G>C	GRCh37
NC_000017.9:g.58908212G>C	NCBI36
NG_011648.1:g.5047G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.25G>C MANE Select	ENSP00000290866.4:p.Gly9Arg
ENST00000290866.9:c.25G>C	ENSP00000290866.4:p.Gly9Arg
ENST00000428043.5:c.25G>C	ENSP00000397593.2:p.Gly9Arg
ENST00000579462.1:n.50G>C
ENST00000582678.5:c.25G>C	ENSP00000462995.1:p.Gly9Arg
ENST00000583336.5:n.59G>C
ENST00000584529.5:n.59G>C
NM_000789.3:c.25G>C	NP_000780.1:p.Gly9Arg
XM_005257110.1:c.-431G>C	XP_005257167.1:n.-431G>C
NM_000789.4:c.25G>C MANE Select	NP_000780.1:p.Gly9Arg
NM_001382700.1:c.-211G>C	NP_001369629.1:n.-211G>C
NM_001382701.1:c.-590G>C	NP_001369630.1:n.-590G>C