Canonical Allele Identifier: CA292870308

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477168A>T , CM000679.2:g.63477168A>T	GRCh38
NC_000017.10:g.61554529A>T , CM000679.1:g.61554529A>T	GRCh37
NC_000017.9:g.58908261A>T	NCBI36
NG_011648.1:g.5096A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.74A>T MANE Select	ENSP00000290866.4:p.Gln25Leu
ENST00000290866.9:c.74A>T	ENSP00000290866.4:p.Gln25Leu
ENST00000428043.5:c.74A>T	ENSP00000397593.2:p.Gln25Leu
ENST00000579462.1:n.99A>T
ENST00000582678.5:c.74A>T	ENSP00000462995.1:p.Gln25Leu
ENST00000583336.5:n.108A>T
ENST00000584529.5:n.108A>T
NM_000789.3:c.74A>T	NP_000780.1:p.Gln25Leu
XM_005257110.1:c.-382A>T	XP_005257167.1:n.-382A>T
NM_000789.4:c.74A>T MANE Select	NP_000780.1:p.Gln25Leu
NM_001382700.1:c.-162A>T	NP_001369629.1:n.-162A>T
NM_001382701.1:c.-541A>T	NP_001369630.1:n.-541A>T