Canonical Allele Identifier: CA2269940275

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478043T= , CM000679.2:g.63478043T=	GRCh38
NC_000017.10:g.61555404T= , CM000679.1:g.61555404T=	GRCh37
NC_000017.9:g.58909136T=	NCBI36
NG_011648.1:g.5971T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.362T= MANE Select	ENSP00000290866.4:p.Ile121=
ENST00000290866.9:c.362T=	ENSP00000290866.4:p.Ile121=
ENST00000428043.5:c.362T=	ENSP00000397593.2:p.Ile121=
ENST00000579462.1:n.387T=
ENST00000580318.1:n.551T=
ENST00000582627.1:c.362T=	ENSP00000462280.1:p.Ile121=
ENST00000582678.5:c.362T=	ENSP00000462995.1:p.Ile121=
ENST00000583336.5:n.396T=
ENST00000584529.5:n.396T=
NM_000789.3:c.362T=	NP_000780.1:p.Ile121=
XM_005257110.1:c.-94T=	XP_005257167.1:n.-94T=
NM_000789.4:c.362T= MANE Select	NP_000780.1:p.Ile121=
NM_001382700.1:c.127T=	NP_001369629.1:p.Ser43=
NM_001382701.1:c.-253T=	NP_001369630.1:n.-253T=