Canonical Allele Identifier: CA8699238

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63480461C>T , CM000679.2:g.63480461C>T	GRCh38
NC_000017.10:g.61557822C>T , CM000679.1:g.61557822C>T	GRCh37
NC_000017.9:g.58911554C>T	NCBI36
NG_011648.1:g.8389C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.780C>T MANE Select	ENSP00000290866.4:p.Arg260=
ENST00000290866.9:c.780C>T	ENSP00000290866.4:p.Arg260=
ENST00000428043.5:c.780C>T	ENSP00000397593.2:p.Arg260=
ENST00000582627.1:c.780C>T	ENSP00000462280.1:p.Arg260=
ENST00000582678.5:c.*179C>T	ENSP00000462995.1:n.*179C>T
ENST00000584529.5:n.814C>T
NM_000789.3:c.780C>T	NP_000780.1:p.Arg260=
XM_005257110.1:c.231C>T	XP_005257167.1:p.Arg77=
NM_000789.4:c.780C>T MANE Select	NP_000780.1:p.Arg260=
NM_001382700.1:c.307C>T	NP_001369629.1:p.Arg103Cys
NM_001382701.1:c.-73C>T	NP_001369630.1:n.-73C>T