Canonical Allele Identifier: CA2269940230

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477950G= , CM000679.2:g.63477950G=	GRCh38
NC_000017.10:g.61555311G= , CM000679.1:g.61555311G=	GRCh37
NC_000017.9:g.58909043G=	NCBI36
NG_011648.1:g.5878G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.269G= MANE Select	ENSP00000290866.4:p.Ser90=
ENST00000290866.9:c.269G=	ENSP00000290866.4:p.Ser90=
ENST00000428043.5:c.269G=	ENSP00000397593.2:p.Ser90=
ENST00000579462.1:n.294G=
ENST00000580318.1:n.458G=
ENST00000582627.1:c.269G=	ENSP00000462280.1:p.Ser90=
ENST00000582678.5:c.269G=	ENSP00000462995.1:p.Ser90=
ENST00000583336.5:n.303G=
ENST00000584529.5:n.303G=
NM_000789.3:c.269G=	NP_000780.1:p.Ser90=
XM_005257110.1:c.-187G=	XP_005257167.1:n.-187G=
NM_000789.4:c.269G= MANE Select	NP_000780.1:p.Ser90=
NM_001382700.1:c.34G=	NP_001369629.1:p.Ala12=
NM_001382701.1:c.-346G=	NP_001369630.1:n.-346G=